Allele Registry

Canonical Allele Identifier: PA2579936996

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.464526875

Score 1.3966646521

Score -1.1991300232

Score 1.4158509158

Linked Data - NCBI & NCI

ClinVar Allele:

363504

ClinVar RCV:

RCV000418417

RCV000419418

RCV000419619

RCV000421674

RCV000423130

RCV000424246

RCV000426827

RCV000428190

RCV000429087

RCV000429251

RCV000434074

RCV000436453

RCV000436660

RCV000438897

RCV000441520

RCV000443007

RCV000471183

RCV000785521

RCV002356517

RCV004022224

ClinVar Variation:

376625

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Lys132Arg	CA16603045 NM_000546.6:c.395A>G