• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Gly244Cys (c.730G>T); ClinVar=VCV000376599; Zygosity=Unspecified (PubMed=22931248; PubMed=28273451).
  

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PubMed=28273451; DOI=10.1016/j.celrep.2017.02.028
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