Canonical Allele Identifier: PA2826567114
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ser176Ile
CA16603075
NM_001276761.3:c.527G>T