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t(1;14)(q21-22;q32)

MedGen UID:: 308371
•Concept ID:: C1515738
•: Cell or Molecular Dysfunction

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(1;14)(q21-22;q32)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Chromosomal translocation
      - t(1;14)(q21-22;q32)

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late embryogenesis abundant protein [Arabidopsis thaliana]
late embryogenesis abundant protein [Arabidopsis thaliana]
Gene ID:818799

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