Canonical Allele Identifier: PA2825745477
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001201
ClinVar RCV Id: RCV001297456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124427.2:p.Glu606Gln
CA403081127
NM_001130955.2:c.1816G>C