Canonical Allele Identifier: PA287785
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Tyr220Cys
CA000315
NM_001126114.3:c.659A>G