Allele Registry

Canonical Allele Identifier: PA2826559925

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418385

RCV000419449

RCV000422508

RCV000427774

RCV000427875

RCV000429067

RCV000430162

RCV000436692

RCV000437360

RCV000437805

RCV000438569

RCV000439724

RCV000443459

RCV000538079

RCV001270273

RCV001567979

RCV002379286

ClinVar Variation:

376599

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Gly205Cys	CA16603021 NM_001276695.3:c.613G>T