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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
12
g.6021960C>A
CA228427
VWF
c.3614G>T (p.Arg1205Leu)
n.421-28026G>T
ClinVar
dbSNP
12
g.6021960C>T
CA114160
VWF
c.3614G>A (p.Arg1205His)
n.421-28026G>A
ClinVar
dbSNP
gnomAD v4
Number of alleles fetched
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