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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPM2
(A262S)
Single nucleotide variant
(missense variant +1 more)
Congenital myopathy 23
GUncertain significance
TPM2
(K48N)
Single nucleotide variant
(missense variant)
Congenital myopathy 23
GUncertain significance