Allele Registry

Canonical Allele Identifier: PA2825483235

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV000080351

RCV001519931

ClinVar Variation:

94379

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075424.1:p.Arg498His	CA147787 NM_001081955.3:c.1493G>A