Allele Registry

Canonical Allele Identifier: PA2826007705

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV000153838

RCV000968923

ClinVar Variation:

167593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159405.1:p.Ser255Leu	CA234791 NM_001165933.2:c.764C>T