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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
12
g.13865797C>A
CA384053400
GRIN2B
c.411+1G>T (n.411+1G>T)
ClinVar
dbSNP
12
g.13865797C>T
CA16609333
GRIN2B
c.411+1G>A (n.411+1G>A)
ClinVar
dbSNP
Number of alleles fetched
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