Allele Registry

Canonical Allele Identifier: PA2579935432

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.8218172313

Score 1.2026855336

Score -0.026337511

Score -0.138075857

Score -0.9589984479

Score 0.558005617

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417479

RCV000419627

RCV000420272

RCV000421524

RCV000421648

RCV000424254

RCV000425630

RCV000426157

RCV000426799

RCV000428146

RCV000428823

RCV000430949

RCV000431481

RCV000432206

RCV000432863

RCV000436862

RCV000437472

RCV000438186

RCV000438677

RCV000438834

RCV000444193

RCV000444980

RCV002356518

RCV002524699

RCV004022237

ClinVar Variation:

376651

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg213Gly	CA16603068 NM_000546.6:c.637C>G