Allele Registry

Canonical Allele Identifier: PA2579935333

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.7678365505

Score 0.324922438

Score -0.038328293

Score 1.6632444149

Score 0.685669665

Score 0.9038614794

Linked Data - NCBI & NCI

ClinVar Allele:

363551

ClinVar RCV:

RCV000418104

RCV000418474

RCV000419558

RCV000423283

RCV000424832

RCV000429571

RCV000429825

RCV000434860

RCV000436131

RCV000439819

RCV000440944

RCV002356519

ClinVar Variation:

376672

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val216Glu	CA16603086 NM_000546.6:c.647T>A