Allele Registry

Canonical Allele Identifier: PA110979

Gene: GABRG2 HGNC NCBI

ClinVar RCV:

RCV000017597

ClinVar Variation:

16211

HGVS (amino-acid)	Matching Registered Transcripts
NP_000807.2:p.Arg177Gly	CA126272 NM_000816.3:c.529C>G