Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149978148G>ACA263269SLC26A2n.728G>A
c.496G>A (p.Gly166Arg)
c.169G>A (p.Gly57Arg)
 ClinVar dbSNP gnomAD v4
5g.149978148G=CA1590737426SLC26A2n.728G=
c.496G= (p.Gly166=)
c.169G= (p.Gly57=)
 dbSNP

Number of alleles fetched