• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Tyr220Cys (c.659A>G); ClinVar=VCV000127819; Zygosity=Unspecified (PubMed=1311061).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Tyr220Ser (c.659A>C); ClinVar=VCV000012383; Zygosity=Unspecified (PubMed=1565469).
  

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