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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.154904518C>A
CA255176
F8
c.5593G>T (p.Asp1865Tyr)
c.5488G>T (p.Asp1830Tyr)
ClinVar
dbSNP
COSMIC
COSMIC
X
g.154904518C>T
CA255175
F8
c.5593G>A (p.Asp1865Asn)
c.5488G>A (p.Asp1830Asn)
ClinVar
dbSNP
Number of alleles fetched
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