Allele Registry

Canonical Allele Identifier: PA2828306137

Gene: ARHGEF9 HGNC NCBI

ClinVar RCV:

RCV000011796

ClinVar Variation:

11049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001355960.1:p.Gly55Ala	CA255660 NM_001369031.1:c.164G>C