Allele Registry

Canonical Allele Identifier: PA2825612818

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363450

ClinVar RCV:

RCV000417784

RCV000417996

RCV000422633

RCV000423257

RCV000425147

RCV000426543

RCV000427160

RCV000432450

RCV000433975

RCV000434565

RCV000434994

RCV000437830

RCV000439618

RCV000442522

RCV000445223

RCV000785535

RCV001023834

RCV003621529

RCV004022204

ClinVar Variation:

376571

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119588.1:p.Cys44Gly	CA16602997 NM_001126116.1:c.130T>G