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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPM1
(D159N +2 more)
Single nucleotide variant
(missense variant)
Familial cardiomyopathy
+5 more
GPathogenic/Likely pathogenic
TPM1
(R160H +2 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+3 more
GPathogenic/Likely pathogenic
TPM1
(E148K +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TPM1
(D230N +2 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+4 more
GPathogenic
TPM1
(E223D +1 more)
Single nucleotide variant
(missense variant +1 more)
Hypertrophic cardiomyopathy 3
+1 more
GUncertain significance
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