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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.5226788A>T
CA125519
HBB
c.104T>A (p.Val35Asp)
n.36T>A
n.155T>A
c.88T>A (p.Ser30Thr)
ClinVar
dbSNP
11
g.5226788A>G
CA217114613
HBB
c.104T>C (p.Val35Ala)
n.36T>C
n.155T>C
c.88T>C (p.Ser30Pro)
dbSNP
Number of alleles fetched
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