• Mutation; HGNC; 11998; TP53; Simple; p.Arg158His (c.473G>A); ClinVar=VCV000141963; Zygosity=Heterozygous (DepMap=ACH-000246).
  
• Mutation; HGNC; 12687; VHL; Simple; p.Trp88Ter (c.264G>A); ClinVar=VCV000936684; Zygosity=Heterozygous (DepMap=ACH-000246).
  

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