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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCP
(T14I)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
+4 more
GUncertain significance
VCP
(D10E)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
GUncertain significance