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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
1
g.209634640T>C
CA16040707
LAMB3
c.373-2A>G (n.373-2A>G)
c.373-1507A>G (n.373-1507A>G)
ClinVar
dbSNP
1
g.209634640T=
CA2484302795
LAMB3
c.373-2A= (n.373-2A=)
c.373-1507A= (n.373-1507A=)
dbSNP
Number of alleles fetched
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