Allele Registry

Canonical Allele Identifier: PA166690

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.989337083

Score 0.661464388

Score -0.201766079

Score 0.490654291

Score 0.052482867

Score 0.147325493

Score 0.359575984

Score 0.608191355

Score -1.1064773217

Score 2.2733315824

Score 1.1719446804

Score 0.653189455

Score 0.6126635

Score 0.712807233

Score 0.679600828

Score 0.205471863

Score 0.181179132

Score 0.730835737

Score 0.86383525

Score 0.450813717

Score 0.142666758

Score 0.225264707

Score 0.060429545

Score 0.286476725

Score 0.563880064

Score 0.180238365

Score 0.590690566

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000130578

RCV000417537

RCV000418238

RCV000423307

RCV000424980

RCV000425504

RCV000426167

RCV000431276

RCV000432429

RCV000432948

RCV000433563

RCV000434278

RCV000435249

RCV000435888

RCV000440994

RCV000443796

RCV000444809

RCV002514731

RCV003237740

RCV003460931

RCV004019741

ClinVar Variation:

141881

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg249Trp	CA000389 NM_000546.6:c.745A>T