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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
15
g.73329725C>T
CA393093935
HCN4
c.1438G>A (p.Gly480Ser)
c.220G>A (p.Gly74Ser)
ClinVar
dbSNP
gnomAD v4
COSMIC
15
g.73329725C>G
CA117313
HCN4
c.1438G>C (p.Gly480Arg)
c.220G>C (p.Gly74Arg)
ClinVar
dbSNP
Number of alleles fetched
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