Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149980653G>TCA16040994SLC26A2c.1060G>T (p.Glu354Ter)
c.372+2302G>T (n.372+2302G>T)
ClinVar dbSNP
5g.149980653G=CA1590738470SLC26A2c.1060G= (p.Glu354=)
c.372+2302G= (n.372+2302G=)
dbSNP

Number of alleles fetched