ID   CENSOi045-A
AC   CVCL_WP52
SY   F202c6
DR   hPSCreg; CENSOi045-A
DR   Wikidata; Q93446785
WW   Provider; Axol; -; https://axolbio.com/shop/disease-models/parkinsons-disease-censoi045-a/
CC   From: Axol Bioscience, Ltd (Censo Biotechnologies); Cambridge; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:11138; SNCA; Simple; p.Gly51Asp (c.152G>A); ClinVar=VCV000097000; Zygosity=Heterozygous (Axol).
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C198602; Parkinson disease 1, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   48Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 10-04-25; Version: 6
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