Allele Registry

Canonical Allele Identifier: PA2579934211

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.348368249

Score 0.241110269

Score -1.162746467

Score 1.0271313678

Score 0.361463777

Linked Data - NCBI & NCI

ClinVar Allele:

363464

ClinVar RCV:

RCV000419187

RCV000419880

RCV000421597

RCV000422382

RCV000422971

RCV000424398

RCV000427237

RCV000429763

RCV000430133

RCV000431847

RCV000432647

RCV000436876

RCV000437480

RCV000438115

RCV000440017

RCV000442319

RCV000442636

RCV000443331

RCV000792342

RCV004022209

ClinVar Variation:

376585

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asp281Tyr	CA16603009 NM_000546.6:c.841G>T