Allele Registry

Canonical Allele Identifier: PA645475241

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.0491481843

Score 0.1509194269

Score 0.0732119179

Score -0.0318199287

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417857

RCV000422141

RCV000424171

RCV000427918

RCV000430043

RCV000430707

RCV000435549

RCV000440979

RCV000662270

RCV002524694

ClinVar Variation:

376323

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly13Ser	CA16602769 NM_005343.4:c.37G>A