ID   ND38548
AC   CVCL_Y817
DR   Coriell; ND38548
DR   NHCDR; ND38548
DR   SKIP; SKIP001091
DR   SKIP; SKIP004706
DR   Wikidata; Q54930070
CC   Sequence variation: Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[42] (c.52CAG(42)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (NHCDR=ND38548).
CC   Discontinued: Coriell; ND38548; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_V568 ! GM04717
SX   Female
AG   44Y
CA   Induced pluripotent stem cell
DT   Created: 10-04-15; Last updated: 30-01-24; Version: 14
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