Canonical Allele Identifier: PA2826559439
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Val118Ala
CA397842041
NM_001276695.3:c.353T>C