• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Tyr126Ter (c.378C>G); ClinVar=VCV000578988; Zygosity=Unspecified (PubMed=16418264).
  

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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=20606684; DOI=10.1038/sj.bjc.6605780; PMCID=PMC2920028
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PubMed=23272949; DOI=10.1186/1755-8794-5-66; PMCID=PMC3543849
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PubMed=29101300; DOI=10.15252/msb.20177701; PMCID=PMC5731344
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