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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNC2
Single nucleotide variant
(missense variant)
Congenital myopathy 15
GPathogenic
TNNC2
Single nucleotide variant
(missense variant)
Congenital myopathy 15
GPathogenic