Allele Registry

Canonical Allele Identifier: PA2579934212

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.107009737

Score 0.9314361615

Score 0.27597724

Score 0.8670409736

Score -1.8331244175

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418744

RCV000419869

RCV000420094

RCV000421295

RCV000422034

RCV000423682

RCV000427301

RCV000427507

RCV000428355

RCV000429459

RCV000429671

RCV000434610

RCV000436837

RCV000437082

RCV000438193

RCV000439019

RCV000439212

RCV000443566

RCV001292542

RCV001306199

RCV002446644

RCV004022210

ClinVar Variation:

376588

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asp281His	CA16603010 NM_000546.6:c.841G>C