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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
1
g.209634506G>A
CA16040705
LAMB3
c.505C>T (p.Gln169Ter)
c.373-1373C>T (n.373-1373C>T)
ClinVar
dbSNP
1
g.209634506G=
CA2484302745
LAMB3
c.505C= (p.Gln169=)
c.373-1373C= (n.373-1373C=)
dbSNP
Number of alleles fetched
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