Canonical Allele Identifier: PA2826567488
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Cys238Phe
CA001518
NM_001276761.3:c.713G>T