Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107674963C>TCA16041104SLC26A4c.619C>T (p.Gln207Ter)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107674963C>GCA368831026SLC26A4c.619C>G (p.Gln207Glu)
dbSNP

Number of alleles fetched