Canonical Allele Identifier: PA2826560896
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Val118Phe
CA000222
NM_001276696.3:c.352G>T