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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLMN, LOC130056366
Single nucleotide variant
(synonymous variant)
CLMN-related disorder
GBenign
CLMN, LOC130056366
(G16R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance