• Mutation; HGNC; 11998; TP53; Simple; p.Tyr234His (c.700T>C); ClinVar=VCV000376691; Zygosity=Unspecified (PubMed=16418264; PubMed=19378335).
  

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PubMed=8464898; DOI=10.1073/pnas.90.7.2842
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PubMed=16418264; DOI=10.1073/pnas.0510146103
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Proc. Natl. Acad. Sci. U.S.A. 103:976-981(2006)

PubMed=18258742; DOI=10.1073/pnas.0712176105
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PubMed=19378335; DOI=10.1002/ijc.24289
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PubMed=20606684; DOI=10.1038/sj.bjc.6605780
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PubMed=29101300; DOI=10.15252/msb.20177701
Frejno M., Zenezini Chiozzi R., Wilhelm M., Koch H., Zheng R.-S., Klaeger S., Ruprecht B., Meng C., Kramer K., Jarzab A., Heinzlmeir S., Johnstone E., Domingo E., Kerr D., Jesinghaus M., Slotta-Huspenina J., Weichert W., Knapp S., Feller S.M., Kuster B.
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