Allele Registry

Canonical Allele Identifier: PA2825483234

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV002002764

ClinVar Variation:

1471896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001075424.1:p.Arg498Leu	CA400673407 NM_001081955.3:c.1493G>T