Allele Registry

Canonical Allele Identifier: PA2579934190

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.2061058037

Score -1.392833758

Score 0.593980969

Score 0.603679283

Score -1.375384829

Score 0.33929823

Score 0.079646361

Score -2.416604129

Score -1.444559719

Score -0.310502662

Score 0.103261386

Score 0.085880313

Score -0.313011672

Score -2.077042149

Score 0.727234516

Score 0.627028549

Score 0.619706805

Score 0.685198957

Score 0.408314801

Score -1.60007363

Score 0.052482867

Score 0.6707063032

Score 0.370963641

Score -3.042045766

Score 0.756397975

Score -1.245549545

Score -0.166545479

Score -2.139628136

Score -1.620515578

Score -0.309104827

Score -2.199001735

Score -0.116443804

Linked Data - NCBI & NCI

ClinVar Allele:

242978

ClinVar RCV:

RCV000226273

RCV000235474

RCV000418376

RCV000421276

RCV000422340

RCV000423658

RCV000425549

RCV000426667

RCV000427734

RCV000428909

RCV000429554

RCV000431918

RCV000433180

RCV000434324

RCV000436164

RCV000437335

RCV000438489

RCV000439593

RCV000442318

RCV000442471

RCV000444806

RCV000492420

RCV000709768

RCV000767028

RCV001357626

RCV003463657

RCV003483584

ClinVar Variation:

237956

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg282Gln	CA10575441 NM_000546.6:c.845G>A