Canonical Allele Identifier: PA2825745253
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 417754
ClinVar RCV Id: RCV000477721 RCV001851127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124427.2:p.Thr216Ala
CA16616861
NM_001130955.2:c.646A>G