Canonical Allele Identifier: PA2829808691
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346227
ClinVar RCV Id: RCV002041370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056133.2:p.Pro507Leu
CA9136901
NM_015318.4:c.1520C>T