Allele Registry

Canonical Allele Identifier: PA103652

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000013439

RCV000353386

ClinVar Variation:

12605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123914.1:p.Lys117Arg	CA256490 NM_001130442.3:c.350A>G