• Mutation; HGNC; HGNC:11998; TP53; Simple; p.Val272Met (c.814G>A); ClinVar=VCV000185814; Zygosity=Homozygous (PubMed=16418264; Cosmic-CLP=924108; DepMap=ACH-002345).
  

CLPUB00026
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PubMed=25926053; DOI=10.1038/ncomms8002
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PubMed=26589293; DOI=10.1186/s13073-015-0240-5; PMCID=PMC4653878
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PubMed=30894373; DOI=10.1158/0008-5472.CAN-18-2747; PMCID=PMC6445675
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Pan-cancer proteomic map of 949 human cell lines.
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