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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
5
g.149980653G>T
CA16040994
SLC26A2
c.1060G>T (p.Glu354Ter)
c.372+2302G>T (n.372+2302G>T)
ClinVar
dbSNP
5
g.149980653G=
CA1590738470
SLC26A2
c.1060G= (p.Glu354=)
c.372+2302G= (n.372+2302G=)
dbSNP
Number of alleles fetched
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