Canonical Allele Identifier: PA2573182431
Gene: ARHGEF18 HGNC NCBI
ClinVar RCV:
RCV001880400
ClinVar Variation:
1356336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124427.2:p.Asn73Ser
CA9136308
NM_001130955.2:c.218A>G