ID   ND41657
AC   CVCL_Y835
DR   Coriell; ND41657
DR   NHCDR; ND41657
DR   SKIP; SKIP001562
DR   SKIP; SKIP004722
DR   Wikidata; Q54930200
CC   Sequence variation: Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[57] (c.52CAG(57)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (NHCDR=ND41657).
CC   Discontinued: Coriell; ND41657; 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_Y897 ! ND33392
SX   Female
AG   29Y
CA   Induced pluripotent stem cell
DT   Created: 10-04-15; Last updated: 19-12-24; Version: 15
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