Allele Registry

Canonical Allele Identifier: PA2826560134

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000214784

RCV000417969

RCV000419043

RCV000421915

RCV000423023

RCV000424153

RCV000428205

RCV000429345

RCV000430442

RCV000433311

RCV000434963

RCV000439555

RCV000440687

RCV000443824

RCV000785311

RCV001042706

RCV001374441

RCV001541668

ClinVar Variation:

232497

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Pro239Leu	CA10580915 NM_001276695.3:c.716C>T