Canonical Allele Identifier: PA2741873361
Gene: ARHGEF18 HGNC NCBI
ClinVar RCV:
RCV003423271
ClinVar Variation:
2649154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354752.1:p.Arg12Trp
CA9136198
NM_001367823.1:c.34C>T