Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.47839727delCA339652CRXc.660del (p.Tyr221ThrfsTer9)
c.*382del (n.*382del)
 ClinVar dbSNP COSMIC
19g.47839727dupCA2339609258CRXc.660dup (p.Tyr221LeufsTer15)
c.*382dup (n.*382dup)
 ClinVar dbSNP

Number of alleles fetched