Canonical Allele Identifier: PA2825618065
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_001119590.1:p.Ser176Arg
CA16603076
NM_001126118.1:c.528T>G
CA397839990
NM_001126118.1:c.528T>A
CA397840019
NM_001126118.1:c.526A>C