Allele Registry

Canonical Allele Identifier: PA2579935155

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.185940956

Score 0.204918672

Score -0.096386241

Score -2.840047926

Score 1.5298575472

Score -0.125269487

Score 0.24356104

Score 0.477508939

Score 0.27233637

Score 0.762914325

Score 0.296256911

Score 0.333951001

Score -1.1136670243

Score 0.494571136

Score 0.39249638

Score 0.318115236

Score 0.522263096

Score 0.296664142

Score 0.299456117

Score 0.099594756

Score 0.287781504

Score 0.045358663

Score 0.478778714

Score 1.1407916128

Score -1.517091858

Score 0.62664078

Score 0.286749714

Linked Data - NCBI & NCI

ClinVar Allele:

260191

ClinVar RCV:

RCV000255018

RCV000420237

RCV000421477

RCV000422531

RCV000425368

RCV000426521

RCV000427619

RCV000428537

RCV000431752

RCV000432804

RCV000433958

RCV000436773

RCV000437884

RCV000438479

RCV000442824

RCV000443789

RCV000443845

RCV002379095

RCV003509522

RCV003995742

ClinVar Variation:

265357

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly245Ala	CA10588670 NM_000546.6:c.734G>C