Allele Registry

Canonical Allele Identifier: PA2579934320

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.7640415268

Score -0.222535539

Score -0.996061277

Score 0.6659057562

Score 0.421311798

Linked Data - NCBI & NCI

ClinVar Allele:

363556

ClinVar RCV:

RCV000420150

RCV000421817

RCV000426067

RCV000426772

RCV000427353

RCV000432482

RCV000433292

RCV000437438

RCV000438006

RCV000443517

RCV000444136

RCV001056029

RCV002429350

ClinVar Variation:

376677

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val274Ala	CA16603091 NM_000546.6:c.821T>C