• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Tyr234His (c.700T>C); ClinVar=VCV000376691; Zygosity=Unspecified (PubMed=16418264; PubMed=19378335).
  

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PubMed=16418264; DOI=10.1073/pnas.0510146103; PMCID=PMC1327731
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PubMed=18258742; DOI=10.1073/pnas.0712176105; PMCID=PMC2268141
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PubMed=19378335; DOI=10.1002/ijc.24289
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PubMed=29101300; DOI=10.15252/msb.20177701; PMCID=PMC5731344
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