Allele Registry

Canonical Allele Identifier: PA2826927467

Gene: ARHGEF10 HGNC NCBI

ClinVar Variation Id: 157538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295081.1:p.His695Tyr	CA270961 NM_001308152.1:c.2083C>T