U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALG13
(I17N)
Single nucleotide variant
(missense variant +2 more)
See cases
+5 more
GLikely pathogenic
ALG13
(E69del)
Microsatellite
(5 prime UTR variant +3 more)
Congenital disorder of glycosylation
GLikely pathogenic
ALG13
(G894V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
Format
Sort by
Choose Destination