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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYBB3
Single nucleotide variant
(intron variant)
Congenital nuclear cataract
+2 more
GBenign
CRYBB3
(H113D)
Single nucleotide variant
(missense variant)
Congenital nuclear cataract
+3 more
GBenign