Allele Registry

Canonical Allele Identifier: PA2579935314

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.440834022

Score 0.753324398

Score 1.727446345

Score 0.5165808795

Score -0.073344682

Score -0.9693724197

Linked Data - NCBI & NCI

ClinVar Allele:

363570

ClinVar RCV:

RCV000418604

RCV000418790

RCV000419222

RCV000421640

RCV000426894

RCV000427499

RCV000428164

RCV000428839

RCV000431867

RCV000436907

RCV000437128

RCV000438411

RCV000439967

RCV000441352

RCV000492782

RCV000530551

RCV000785304

RCV002289544

ClinVar Variation:

376691

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr234His	CA16603104 NM_000546.6:c.700T>C