Canonical Allele Identifier: PA2828273799
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 1951050
ClinVar RCV Id: RCV002681695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354753.1:p.Arg473Trp
CA304853694
NM_001367824.1:c.1417C>T