ID   GM26582
AC   CVCL_RT69
DR   Coriell; GM26582
DR   Wikidata; Q54854101
CC   Sequence variation: Mutation; HGNC; HGNC:17646; NGLY1; Simple; p.Arg401Ter (c.1201A>T); ClinVar=VCV000050962; Zygosity=Heterozygous (Coriell=GM26582).
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_BX26 ! GM25342
SX   Male
AG   32Y
CA   Finite cell line
DT   Created: 05-03-18; Last updated: 19-12-24; Version: 11
//