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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
5
g.45396550C>T
CA16044317
HCN1
c.1172G>A (p.Gly391Asp)
n.335G>A
ClinVar
dbSNP
COSMIC
5
g.45396550C>A
CA359705262
HCN1
c.1172G>T (p.Gly391Val)
n.335G>T
ClinVar
dbSNP
Number of alleles fetched
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