Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107674337G>TCA368848422SLC26A4c.589G>T (p.Gly197Ter)
 ClinVar dbSNP
7g.107674337G>ACA261433SLC26A4c.589G>A (p.Gly197Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched