Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.90749850delCA344541BLMc.582del (p.Phe194LeufsTer11)
n.756del
c.-710del (n.-710del)
 ClinVar dbSNP
15g.90749849_90749850delCA274291BLMc.581_582del (p.Phe194Ter)
n.755_756del
c.-711_-710del (n.-711_-710del)
 ClinVar dbSNP ExAC gnomAD v4

Number of alleles fetched