Canonical Allele Identifier: PA2826561157
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Tyr166Asp
CA16603100
NM_001276696.3:c.496T>G