• Mutation; HGNC; HGNC:7882; NOTCH2; Simple; p.Gly49Glu (c.146G>A); Zygosity=Unspecified (PubMed=24662767).
  
• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg267Pro (c.800G>C); ClinVar=VCV000428867; Zygosity=Unspecified (PubMed=24662767).
  

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