Canonical Allele Identifier: PA2825745466
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 846258
ClinVar RCV Id: RCV001049516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124427.2:p.Ala586Thr
CA9136879
NM_001130955.2:c.1756G>A