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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NODAL
(V208L +1 more)
Single nucleotide variant
(missense variant)
congenital heart defects
GUncertain significance
NODAL
(D135G +1 more)
Single nucleotide variant
(missense variant)
Heterotaxy, visceral, 5, autosomal
GUncertain significance