Allele Registry

Canonical Allele Identifier: PA2579934210

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.2894015

Score -0.3288429954

Score 0.5831352992

Score -1.7536360224

Score -0.913859855

Linked Data - NCBI & NCI

ClinVar Allele:

363468

ClinVar RCV:

RCV000417517

RCV000419849

RCV000420104

RCV000422679

RCV000424893

RCV000425979

RCV000427537

RCV000429708

RCV000430790

RCV000433406

RCV000435611

RCV000435784

RCV000438210

RCV000440361

RCV000440602

RCV000442214

RCV000442965

RCV000443934

RCV003463826

ClinVar Variation:

376589

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asp281Ala	CA16603011 NM_000546.6:c.842A>C