Allele Registry

Canonical Allele Identifier: PA106980

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.3663558957

Score 0.4858100383

Score 0.252885223

Score 0.249307121

Score 1.8254665341

Score 0.216807505

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417831

RCV000420188

RCV000423073

RCV000424338

RCV000428522

RCV000430897

RCV000433321

RCV000433805

RCV000434977

RCV000439173

RCV000440310

RCV000441607

RCV000443964

RCV000785338

RCV004022214

ClinVar Variation:

376601

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly244Val	CA16603023 NM_000546.6:c.731G>T