Allele Registry

Canonical Allele Identifier: PA114822

Gene: ARHGAP9 HGNC NCBI

ClinVar RCV:

RCV000001248

ClinVar Variation:

1189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073625.1:p.Ser186Ala	CA114821 NM_001080156.3:c.556T>G