ID   CENSOi017-A
AC   CVCL_VC71
SY   F190c12b
DR   BioSamples; SAMEA994016
DR   hPSCreg; CENSOi017-A
DR   Wikidata; Q54809309
WW   Provider; Axol; -; https://axolbio.com/shop/disease-models/huntingtons-disease/huntingtons-disease-censoi017-a/
CC   From: Axol Bioscience, Ltd (Censo Biotechnologies); Cambridge; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[~42] (c.52CAG(~42)) (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)
SX   Female
AG   51Y
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 10-04-25; Version: 6
//