Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149980292G>CCA263275SLC26A2c.700-1G>C (n.700-1G>C)
c.372+1941G>C (n.372+1941G>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
5g.149980292G=CA1590738294SLC26A2c.700-1G= (n.700-1G=)
c.372+1941G= (n.372+1941G=)
dbSNP

Number of alleles fetched