Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107674163G>ACA16041102SLC26A4c.416-1G>A (n.416-1G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107674163G=CA1732745864SLC26A4c.416-1G= (n.416-1G=)
dbSNP

Number of alleles fetched