Canonical Allele Identifier: PA2825745479
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 1901018
ClinVar RCV Id: RCV002586075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124427.2:p.Asp607Glu
CA9136896
NM_001130955.2:c.1821C>A
CA403081151
NM_001130955.2:c.1821C>G