ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
11
g.102798499A>G
CA13394799
WTAPP1
n.423+377A>G
n.682+377A>G
n.443+377A>G
ClinVar
dbSNP
gnomAD v2
gnomAD v3
gnomAD v4
11
g.102798499A=
CA2573050022
WTAPP1
n.423+377A=
n.682+377A=
n.443+377A=
dbSNP
Number of alleles fetched
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