Allele Registry

Canonical Allele Identifier: PA645475180

Gene: HRAS HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.0610389236

Score 0.0009136261

Score 0.0978672622

Score 0.1623644246

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421384

RCV000424186

RCV000425652

RCV000426316

RCV000433957

RCV000434248

RCV000434457

RCV000440965

RCV000442365

RCV000445345

ClinVar Variation:

376443

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005334.1:p.Gly13Ala	CA16602878 NM_005343.4:c.38G>C