Allele Registry

Canonical Allele Identifier: PA2579935490

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.3283654357

Score 1.2901032565

Score 1.2528399815

Score 0.273163204

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421312

RCV000421805

RCV000422467

RCV000426991

RCV000427622

RCV000429226

RCV000429901

RCV000431547

RCV000432185

RCV000437242

RCV000437865

RCV000439461

RCV000440129

RCV000442296

RCV000442729

RCV000445057

RCV001184465

RCV004022221

ClinVar Variation:

376619

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ile195Ser	CA16603039 NM_000546.6:c.584T>G