CASLcDB
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Family
ALL
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Region
ALL
R1
R2
R3
R4
R5
Clinical significance
Risk_factor
Pathogenic
Likely_pathogenic
Benign
Likely_benign
Affects
Association
not_provided
Uncertain_significance
Topology & Mutation
Mutation Data
SLC name
Type
Significance
Criteria
Disease
Seq start
Seq end
Seq original
Seq new
AA start
AA end
AA original
AA new
Region
Var ID
Allele ID
Chr
Loc
Assmbl