Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149981044G>ACA263252SLC26A2c.1451G>A (p.Gly484Asp)
c.372+2693G>A (n.372+2693G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
5g.149981044G=CA1590738626SLC26A2c.1451G= (p.Gly484=)
c.372+2693G= (n.372+2693G=)
dbSNP

Number of alleles fetched