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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.5226997T>C
CA125050
HBB
c.25A>G (p.Lys9Glu)
n.76A>G
ClinVar
dbSNP
11
g.5226997T>G
CA124959
HBB
c.25A>C (p.Lys9Gln)
n.76A>C
ClinVar
dbSNP
Number of alleles fetched
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