Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149977707G>TCA263272SLC26A2n.287G>T
c.55G>T (p.Gly19Ter)
 ClinVar dbSNP gnomAD v4
5g.149977707G=CA1590737249SLC26A2n.287G=
c.55G= (p.Gly19=)
 dbSNP

Number of alleles fetched