ID   PFIZi032-A
AC   CVCL_VE80
SY   B214c8
DR   BioSamples; SAMEA104494774
DR   EBiSC; PFIZi032-A
DR   ECACC; 66540885
DR   hPSCreg; PFIZi032-A
DR   Wikidata; Q54947298
CC   From: Pfizer, Inc.; New York; USA.
CC   Sequence variation: Mutation; HGNC; HGNC:12363; TSC2; Unexplicit; Not described; Zygosity=Unspecified (EBiSC=PFIZi032-A).
CC   Discontinued: ECACC; 66540885; true.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C116573; Dravet syndrome
DI   ORDO; Orphanet_33069; Dravet syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 14-05-18; Last updated: 19-12-24; Version: 10
//