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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCT
(S34R)
Single nucleotide variant
(missense variant +1 more)
Oculocutaneous albinism type 8
GUncertain significance
DCT
(N129I +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GLikely pathogenic