Canonical Allele Identifier: PA2826567117
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ser176Cys
CA397840015
NM_001276761.3:c.526A>T