Canonical Allele Identifier: PA2829808636
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 971686
ClinVar RCV Id: RCV001247520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056133.2:p.Met476Val
CA9136876
NM_015318.4:c.1426A>G