Canonical Allele Identifier: PA1139741557
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 971686
ClinVar RCV Id: RCV001247520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354752.1:p.Met822Val
CA9136876
NM_001367823.1:c.2464A>G