Allele Registry

Canonical Allele Identifier: PA2825604599

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421044

RCV000422178

RCV000425174

RCV000431745

RCV000432876

RCV000437603

RCV000439391

RCV000442610

RCV000442691

RCV000465501

RCV000492567

RCV000662560

RCV000785463

RCV002289537

RCV002523445

RCV002857438

RCV004023282

ClinVar Variation:

376661

428895

2020649

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119585.1:p.Ser215Arg	CA16603076 NM_001126113.3:c.645T>G CA397839990 NM_001126113.3:c.645T>A CA397840019 NM_001126113.3:c.643A>C