Allele Registry

Canonical Allele Identifier: PA107082

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.139652744

Score 1.2400516469

Score 0.9355709948

Score -0.8718036977

Score 0.939032004

Linked Data - NCBI & NCI

ClinVar Allele:

27389

ClinVar RCV:

RCV000013143

RCV001213570

RCV003237412

ClinVar Variation:

12350

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Leu252Pro	CA000398 NM_000546.6:c.755T>C