ID   HPS3216
AC   CVCL_C6DQ
DR   RCB; HPS3216
DR   Wikidata; Q116049501
CC   Sequence variation: Mutation; HGNC; HGNC:6192; JAK2; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS3216).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C27701; Secondary myelofibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C6DP ! HPS3215
OI   CVCL_C6DR ! HPS3217
SX   Female
AG   70-79Y
CA   Induced pluripotent stem cell
DT   Created: 15-12-22; Last updated: 19-12-24; Version: 4
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