Allele Registry

Canonical Allele Identifier: PA166332

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.7559270965

Score 0.186819063

Score -0.8121334073

Score 1.5165709279

Linked Data - NCBI & NCI

ClinVar Allele:

151476

ClinVar RCV:

RCV000130396

RCV000419337

RCV000419825

RCV000421166

RCV000422242

RCV000423651

RCV000428748

RCV000429447

RCV000430048

RCV000431855

RCV000437052

RCV000438381

RCV000439440

RCV000444676

RCV000581322

RCV001069143

RCV004019738

ClinVar Variation:

141762

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys135Tyr	CA000160 NM_000546.6:c.404G>A