Allele Registry

Canonical Allele Identifier: PA2579936039

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.18050116

Score -1.0009905826

Score 1.0457041618

Score 1.9427124924

Linked Data - NCBI & NCI

ClinVar Allele:

363558

ClinVar RCV:

RCV000421406

RCV000422095

RCV000424159

RCV000426404

RCV000427021

RCV000428833

RCV000431660

RCV000434430

RCV000437297

RCV000439053

RCV000439742

RCV000443298

RCV000443877

RCV000444003

RCV000633347

RCV002338982

RCV004022250

ClinVar Variation:

376679

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr163Asn	CA16603093 NM_000546.6:c.487T>A