Canonical Allele Identifier: PA2825745482
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346227
ClinVar RCV Id: RCV002041370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124427.2:p.Pro611Leu
CA9136901
NM_001130955.2:c.1832C>T