Allele Registry

Canonical Allele Identifier: PA658828619

Gene: HRAS HGNC NCBI

Linked Data

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_789765.1:p.Gly13Ser	CA16602769 NM_176795.5:c.37G>A