ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
19
g.7526607G>C
CA403081028
MCOLN1
c.405+1G>C (n.405+1G>C)
n.485+1G>C
n.367+1G>C
n.226+1G>C
ClinVar
dbSNP
19
g.7526607G>A
CA9138706
MCOLN1
c.405+1G>A (n.405+1G>A)
n.485+1G>A
n.367+1G>A
n.226+1G>A
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v3
gnomAD v4
Number of alleles fetched
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