Allele Registry

Canonical Allele Identifier: PA2826007696

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV000171265

ClinVar Variation:

191085

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159405.1:p.Ala232Val	CA235987 NM_001165933.2:c.695C>T