Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107690178G>ACA261400SLC26A4c.1204G>A (p.Val402Met)
 ClinVar dbSNP gnomAD v4
7g.107690178G=CA1732748321SLC26A4c.1204G= (p.Val402=)
 dbSNP

Number of alleles fetched