Canonical Allele Identifier: PA2826565598
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376661
ClinVar Variation Id: 428895
ClinVar Variation Id: 2020649
ClinVar RCV Id: RCV002857438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser176Arg
CA16603076
NM_001276760.3:c.528T>G
CA397839990
NM_001276760.3:c.528T>A
CA397840019
NM_001276760.3:c.526A>C