OnlineIMD
Cystinuria type B
Type
Disease
External link(s)
Orphanet
IEMbase
VMH
Gene
SLC7A9
/ Solute Carrier Family 7 Member 9
19q13.11
OMIM
GnomAD
Ensembl
HGNC
VMH
LOVD
Gene product
Cystine/basic amino acid transporter
Parent entry
Cystinuria