Canonical Allele Identifier: PA916050380
Gene: ARHGAP18 HGNC NCBI

Linked Data

ClinVar Variation Id: 783473
ClinVar RCV Id: RCV000965020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277050.2:p.Gly32Arg
CA3995776
NM_033515.3:c.94G>A
CA365829816
NM_033515.3:c.94G>C