Allele Registry

Canonical Allele Identifier: PA256489

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.2543448961

Score 0.0610686109

Score 0.0816774606

Score 0.3927024248

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013438

RCV000157913

RCV000439514

RCV000781469

RCV001376018

RCV001813187

RCV002476960

RCV003390677

ClinVar Variation:

12604

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly13Asp	CA256488 NM_005343.4:c.38G>A