Allele Registry

Canonical Allele Identifier: PA107119

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.6560708419

Score 0.9685675495

Score -0.5070290105

Score 0.475880861

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417803

RCV000417874

RCV000423644

RCV000425237

RCV000426379

RCV000428580

RCV000430828

RCV000431096

RCV000433855

RCV000434893

RCV000435981

RCV000436180

RCV000440656

RCV000441816

RCV000442199

RCV000444903

RCV000468362

RCV000562533

RCV001253548

RCV004017609

ClinVar Variation:

376626

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Lys132Glu	CA002647 NM_000546.6:c.394A>G