Canonical Allele Identifier: PA2825614190
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 422130
ClinVar Variation Id: 925213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119588.1:p.Glu155Asp
CA001463
NM_001126116.1:c.465G>C
CA397836649
NM_001126116.1:c.465G>T