OPEDVar

QUERY TYPE AlleleID GeneID GeneSymbol HGNC_ID Select query type and 'AlleleID','GeneID',
'GeneSymbol' and 'HGNC_ID' QUERY ITEM Enter the AlleleID,GeneID,GeneSymbol or HGNC_ID PAM NGG NG Select PAM type between 'NGG' and 'NG' DIRECTION install correct Select edit direction which means to install
or correct pathogenic human genetic variants ASSEMBLY GRch38 HISTORY