Allele Registry

Canonical Allele Identifier: PA2579935199

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.191793391

Score -0.0000384

Score 1.6593156072

Score 0.4546801525

Score -0.8209235544

Score 0.275668808

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419348

RCV000420409

RCV000421679

RCV000421933

RCV000424052

RCV000426193

RCV000428210

RCV000430482

RCV000430655

RCV000431946

RCV000433046

RCV000437018

RCV000437199

RCV000438447

RCV000441834

RCV000441879

RCV000442237

RCV000492666

RCV000812726

RCV002289521

ClinVar Variation:

376576

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys238Arg	CA16603002 NM_000546.6:c.712T>C