Allele Registry

Canonical Allele Identifier: PA645475331

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.3378042126

Score 0.3962226311

Score 0.0095294637

Score -0.0040079065

Linked Data - NCBI & NCI

ClinVar Allele:

363197

363198

ClinVar RCV:

RCV000420806

RCV000421964

RCV000423449

RCV000424686

RCV000428014

RCV000433099

RCV000433734

RCV000434965

RCV000440259

RCV000442468

RCV000444731

RCV000589258

ClinVar Variation:

376318

376319

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gln61His	CA16602764 NM_005343.4:c.183G>T CA16602765 NM_005343.4:c.183G>C