Allele Registry

Canonical Allele Identifier: PA645475338

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.3443139705

Score 0.1923342085

Score 0.0408954161

Score -0.0319742929

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417619

RCV000419094

RCV000420448

RCV000424105

RCV000425877

RCV000428681

RCV000428741

RCV000430030

RCV000430658

RCV000435275

RCV000435489

RCV000435915

RCV000440764

RCV000441832

ClinVar Variation:

376322

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gln61Pro	CA16602768 NM_005343.4:c.182A>C