Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107663301C>ACA4432386SLC26A4c.170C>A (p.Ser57Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.107663301C>GCA261419SLC26A4c.170C>G (p.Ser57Ter)
 ClinVar dbSNP

Number of alleles fetched