Allele Registry

Canonical Allele Identifier: PA193063

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.6747168308

Score 0.586577077

Score 0.094335382

Score 1.1374321088

Score -1.0502491134

Linked Data - NCBI & NCI

ClinVar Allele:

185366

ClinVar RCV:

RCV000165315

RCV000419701

RCV000420523

RCV000421145

RCV000421777

RCV000422830

RCV000426960

RCV000427615

RCV000428359

RCV000430839

RCV000431198

RCV000432479

RCV000433537

RCV000437609

RCV000437660

RCV000438323

RCV000438373

RCV000439007

RCV000441921

RCV000443734

RCV000444673

RCV000697802

RCV000785542

RCV004019975

ClinVar Variation:

185822

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.His193Leu	CA000276 NM_000546.6:c.578A>T