Canonical Allele Identifier: PA287672
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127810
ClinVar RCV Id: RCV000115721 RCV000213051 RCV000232885 RCV000409094 RCV000764146 RCV002465516 RCV003467058
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Arg24Cys
CA000214
NM_001126117.1:c.70C>T