Allele Registry

Canonical Allele Identifier: PA2579936995

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.0118779362

Score 0.7097338127

Score -0.7163725822

Score -0.154917513

Linked Data - NCBI & NCI

ClinVar Allele:

363508

ClinVar RCV:

RCV000418504

RCV000418722

RCV000421596

RCV000424301

RCV000426255

RCV000426873

RCV000428123

RCV000428765

RCV000431846

RCV000433916

RCV000434568

RCV000437107

RCV000438364

RCV000439874

RCV000441135

RCV000442900

RCV000546420

ClinVar Variation:

376629

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Lys132Met	CA16603048 NM_000546.6:c.395A>T