Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107690238G>ACA16041109SLC26A4c.1263+1G>A (n.1263+1G>A)
ClinVar dbSNP gnomAD v4
7g.107690238G>TCA16041110SLC26A4c.1263+1G>T (n.1263+1G>T)
ClinVar dbSNP

Number of alleles fetched