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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.5227018C>T
CA125180
HBB
c.4G>A (p.Val2Met)
n.55G>A
ClinVar
dbSNP
gnomAD v2
gnomAD v4
11
g.5227018C>A
CA125444
HBB
c.4G>T (p.Val2Leu)
n.55G>T
ClinVar
dbSNP
gnomAD v4
Number of alleles fetched
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