Allele Registry

Canonical Allele Identifier: PA106861

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.6051165573

Score 0.8574274322

Score 0.457132304

Score -0.002384322

Score 1.1150026024

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418705

RCV000421233

RCV000422096

RCV000424002

RCV000426180

RCV000426863

RCV000428837

RCV000428968

RCV000429505

RCV000431489

RCV000434267

RCV000436424

RCV000437075

RCV000438896

RCV000439749

RCV000442054

RCV000443405

RCV000443489

RCV000785452

RCV000824609

RCV002446642

ClinVar Variation:

376586

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asp281Asn	CA001503 NM_000546.6:c.841G>A