Allele Registry

Canonical Allele Identifier: PA916024330

Gene: ARHGAP9 HGNC NCBI

ClinVar RCV:

RCV000001248

ClinVar Variation:

1189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001306780.1:p.Ser40Ala	CA114821 NM_001319851.2:c.118T>G