Allele Registry

Canonical Allele Identifier: PA2579934227

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.8251806647

Score -0.522323347

Score -1.2143134089

Score 1.2504185205

Score 0.109282927

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418465

RCV000419917

RCV000420625

RCV000421324

RCV000424417

RCV000426479

RCV000427170

RCV000429590

RCV000430194

RCV000431582

RCV000435565

RCV000436708

RCV000438255

RCV000439157

RCV000439619

RCV000439812

RCV000445156

RCV000568150

RCV000706131

RCV000785300

RCV003476010

RCV004022240

ClinVar Variation:

376658

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg280Gly	CA16603073 NM_000546.6:c.838A>G