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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC114004369, NCL
(T707M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC114004369, NCL
Single nucleotide variant
(intron variant)
not provided
GBenign