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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TUBB6
(E125D +3 more)
Single nucleotide variant
(missense variant +2 more)
Facial palsy, congenital, with ptosis and velopharyngeal dysfunction
GUncertain significance
TUBB6
(E264K +4 more)
Single nucleotide variant
(missense variant +1 more)
Facial palsy, congenital, with ptosis and velopharyngeal dysfunction
GUncertain significance