Canonical Allele Identifier: PA916046958
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_001354752.1:p.Thr458Ala
CA16616861
NM_001367823.1:c.1372A>G