Allele Registry

Canonical Allele Identifier: PA235988

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV000171265

ClinVar Variation:

191085

HGVS (amino-acid)	Matching Registered Transcripts
NP_003826.2:p.Ala235Val	CA235987 NM_003835.4:c.704C>T