Canonical Allele Identifier: PA2826567116
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ser176Asn
CA16603077
NM_001276761.3:c.527G>A