Allele Registry

Canonical Allele Identifier: PA2828233598

Gene: ARHGAP9 HGNC NCBI

ClinVar RCV:

RCV000001248

ClinVar Variation:

1189

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354354.1:p.Ser155Ala	CA114821 NM_001367425.1:c.463T>G