Canonical Allele Identifier: PA2826565601
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 265337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser176Gly
CA10588671
NM_001276760.3:c.526A>G