Allele Registry

Canonical Allele Identifier: PA114823

Gene: ARHGAP9 HGNC NCBI

ClinVar RCV:

RCV000001248

ClinVar Variation:

1189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073626.1:p.Ser370Ala	CA114821 NM_001080157.2:c.1108T>G