Allele Registry

Canonical Allele Identifier: PA2579935491

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.0145762818

Score 0.4597954805

Score 1.6227819217

Score 0.113558855

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417492

RCV000419606

RCV000420311

RCV000422932

RCV000424894

RCV000425779

RCV000427719

RCV000430554

RCV000432578

RCV000433212

RCV000435160

RCV000437965

RCV000440578

RCV000440765

RCV000442006

RCV000444669

RCV000692717

RCV000785514

RCV001024599

RCV002289528

ClinVar Variation:

376618

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ile195Asn	CA16603038 NM_000546.6:c.584T>A CA3054203864 NM_000546.6:c.584_585delinsAT