Allele Registry

Canonical Allele Identifier: PA2573234628

Gene: RGS9 HGNC NCBI

ClinVar RCV:

RCV002002764

ClinVar Variation:

1471896

HGVS (amino-acid)	Matching Registered Transcripts
NP_003826.2:p.Arg501Leu	CA400673407 NM_003835.4:c.1502G>T