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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130057162, SLTM
(A13T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130057162, SLTM
(A10P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance