Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107689136C>ACA16042657SLC26A4c.1085C>A (p.Ala362Asp)
ClinVar dbSNP
7g.107689136C=CA1732747373SLC26A4c.1085C= (p.Ala362=)
dbSNP

Number of alleles fetched