• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Gly245Ser (c.733G>A); ClinVar=VCV000012365; Zygosity=Homozygous (PubMed=11107048; Cosmic-CLP=1322224; DepMap=ACH-002141).
  

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Pathol. Int. 50:767-777(2000)

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