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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
12
g.6018877A>C
CA114154
VWF
c.4541T>G (p.Phe1514Cys)
n.421-24943T>G
ClinVar
dbSNP
12
g.6018877A=
CA2013872719
VWF
c.4541T= (p.Phe1514=)
n.421-24943T=
dbSNP
Number of alleles fetched
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