• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Ile251Leu (c.751A>C); ClinVar=VCV000182937; Zygosity=Unspecified (PubMed=1370612; PubMed=11107048; PubMed=15900046; PubMed=15901131; PubMed=22490663).
  

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