Allele Registry

Canonical Allele Identifier: PA106690

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.5983644492

Score 0.043879442

Score -0.140239594

Score 1.4806803903

Score -0.531062544

Score -0.5156480164

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000220461

RCV000418520

RCV000419521

RCV000420213

RCV000423147

RCV000423776

RCV000424407

RCV000425014

RCV000426111

RCV000429975

RCV000430230

RCV000430895

RCV000431639

RCV000433848

RCV000434458

RCV000435742

RCV000436779

RCV000440212

RCV000440917

RCV000441029

RCV000441598

RCV000443850

RCV000443926

RCV000506128

RCV002288865

RCV002518297

ClinVar Variation:

231214

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg213Pro	CA10580932 NM_000546.6:c.638G>C