VCV000788465.2 - ClinVar - NCBI
NM_015318.4(ARHGEF18):c.1671C>T (p.Se7=) Allele ID 716762 Variant type single nucleotide variant Variant length 1 bp Cytogenetic location 19p13.2 Genomic location 19: 7463891 (GRCh38) GRCh38 UCSC 19: 7528777 (GRCh37 ...