Allele Registry

Canonical Allele Identifier: PA2579936492

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.9758268732

Score 0.6454091307

Score 1.0789128483

Score -0.566753466

Score -0.840210526

Linked Data - NCBI & NCI

ClinVar Allele:

363441

ClinVar RCV:

RCV000420576

RCV000422226

RCV000424613

RCV000426276

RCV000426947

RCV000430830

RCV000431837

RCV000432917

RCV000437180

RCV000438245

RCV000443653

RCV000444857

RCV000444883

RCV000814994

ClinVar Variation:

376562

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys135Ser	CA16602988 NM_000546.6:c.403T>A CA397842777 NM_000546.6:c.404G>C