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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.5225651A>C
CA125233
HBB
c.391T>G (p.Tyr131Asp)
c.*207T>G (n.*207T>G)
ClinVar
dbSNP
11
g.5225651A=
CA1949564594
HBB
c.391T= (p.Tyr131=)
c.*207T= (n.*207T=)
dbSNP
Number of alleles fetched
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