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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYPN
(V532M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
MYPN
(R955W +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MYPN
Single nucleotide variant
(intron variant)
Dilated cardiomyopathy 1KK
GUncertain significance
MYPN
(R1278Q +1 more)
Single nucleotide variant
(missense variant +1 more)
MYPN-related myopathy
+4 more
GConflicting classifications of pathogenicity
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