U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MCM3AP
(Q1159fs)
Deletion
(frameshift variant)
not provided
+3 more
GPathogenic
MCM3AP
(L882F)
Single nucleotide variant
(missense variant)
Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development
GUncertain significance