Allele Registry

Canonical Allele Identifier: PA916022166

Gene: HRAS HGNC NCBI

ClinVar RCV:

RCV000013439

RCV000353386

ClinVar Variation:

12605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304983.1:p.Ser11Gly	CA256490 NM_001318054.2:c.31A>G