Allele Registry

Canonical Allele Identifier: PA234792

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV000153838

RCV000968923

ClinVar Variation:

167593

HGVS (amino-acid)	Matching Registered Transcripts
NP_003826.2:p.Ser258Leu	CA234791 NM_003835.4:c.773C>T