Allele Registry

Canonical Allele Identifier: PA2579935963

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.079493189

Score 0.0739290214

Score 0.1855620186

Score 0.355449461

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418067

RCV000419091

RCV000419301

RCV000422109

RCV000422797

RCV000424599

RCV000424807

RCV000427824

RCV000429415

RCV000430449

RCV000433494

RCV000433706

RCV000434154

RCV000434865

RCV000435925

RCV000440508

RCV000440898

RCV000444321

RCV000445154

RCV000564826

RCV000695193

RCV001575036

RCV004022218

ClinVar Variation:

376609

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.His179Asn	CA16603030 NM_000546.6:c.535C>A