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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYLK2
(P39L)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+1 more
GUncertain significance
MYLK2
(G64A)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MYLK2
(A102V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MYLK2
(R340H)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+1 more
GUncertain significance
MYLK2
(R549C)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+1 more
GUncertain significance
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