Allele Registry

Canonical Allele Identifier: PA147788

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV000080351

RCV001519931

ClinVar Variation:

94379

HGVS (amino-acid)	Matching Registered Transcripts
NP_003826.2:p.Arg501His	CA147787 NM_003835.4:c.1502G>A