Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107674350T>ACA16041103SLC26A4c.600+2T>A (n.600+2T>A)
ClinVar dbSNP
7g.107674350T>CCA368848470SLC26A4c.600+2T>C (n.600+2T>C)
ClinVar dbSNP

Showing alleles 1 - 2 from query results