Allele Registry

Canonical Allele Identifier: PA2579935961

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.0579753597

Score 0.223426773

Score -0.3938178085

Score 0.2206567701

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417695

RCV000417973

RCV000420789

RCV000421853

RCV000423292

RCV000426502

RCV000427175

RCV000428674

RCV000429260

RCV000432550

RCV000433227

RCV000433943

RCV000437826

RCV000438042

RCV000438407

RCV000439947

RCV000440632

RCV000443785

RCV000445268

RCV000529132

RCV000785555

RCV001023983

RCV001591055

RCV003983035

RCV004022216

ClinVar Variation:

376606

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.His179Arg	CA16603027 NM_000546.6:c.536A>G