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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
14
g.28768034G>A
CA389475799
FOXG1
c.755G>A (p.Gly252Asp)
ClinVar
dbSNP
14
g.28768034G>T
CA172191
FOXG1
c.755G>T (p.Gly252Val)
ClinVar
dbSNP
Number of alleles fetched
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