Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107683355G>TCA261444SLC26A4c.918+1G>T (n.918+1G>T)
 ClinVar dbSNP
7g.107683355G>CCA368835552SLC26A4c.918+1G>C (n.918+1G>C)
 ClinVar dbSNP gnomAD v4

Number of alleles fetched