Allele Registry

Canonical Allele Identifier: PA2579934577

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 2.0427638746

Score 0.761193961

Score 0.510245963

Score 1.021944396

Score 0.705538915

Score 0.503023701

Score -1.2450171835

Score 1.3088444499

Score 0.379812599

Score 0.166905356

Score -0.198174994

Score 0.701691852

Score -0.330190655

Score 0.852644299

Score -1.245549545

Score -0.018456137

Score 0.581798519

Score 0.143403316

Score 0.837505509

Score 0.649789617

Score 0.44744136

Score 0.783669602

Linked Data - NCBI & NCI

ClinVar Allele:

362894

ClinVar RCV:

RCV000420349

RCV000422597

RCV000423288

RCV000424367

RCV000425028

RCV000426063

RCV000430687

RCV000431816

RCV000432872

RCV000433555

RCV000438147

RCV000440254

RCV000440948

RCV000441532

RCV000444506

RCV000444945

RCV000445262

RCV001311109

RCV002392945

RCV004022197

ClinVar Variation:

376015

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg249Thr	CA16602484 NM_000546.6:c.746G>C