Allele Registry

Canonical Allele Identifier: PA2579934322

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.921822075

Score -0.496700133

Score 0.592861446

Score -1.5252985443

Score 1.4726874733

Linked Data - NCBI & NCI

ClinVar Allele:

363557

ClinVar RCV:

RCV000418040

RCV000420871

RCV000422166

RCV000422877

RCV000428087

RCV000428696

RCV000429377

RCV000433566

RCV000435261

RCV000439367

RCV000440106

RCV000701251

ClinVar Variation:

376678

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val274Leu	CA16603092 NM_000546.6:c.820G>C