ID   CENSOi011-D
AC   CVCL_E4FQ
WW   https://axolbio.com/shop/disease-models/huntingtons-disease/huntingtons-disease-censoi011-d/
CC   From: Axol Bioscience Ltd. (Censo Biotechnologies); Cambridge; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[39] (c.52CAG(39)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (Axol).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_E3T0 ! CENSOi011-A
OI   CVCL_VC66 ! CENSOi011-B
SX   Female
AG   40-50Y
CA   Induced pluripotent stem cell
DT   Created: 19-12-24; Last updated: 19-12-24; Version: 1
//