Allele Registry

Canonical Allele Identifier: PA191629

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.5413034882

Score 0.4650645642

Score -0.062554556

Score -1.0249800693

Score 0.426838079

Linked Data - NCBI & NCI

ClinVar Allele:

185349

ClinVar RCV:

RCV000164718

RCV003765021

ClinVar Variation:

185319

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ala276Gly	CA000436 NM_000546.6:c.827C>G