KIT c.856G>C ;(p.G286R)

Variant ID: 4-55569989-G-C

NM_000222.2(KIT):c.856G>C;(p.G286R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics.

Immunology
Haenisch, Britta B; Nöthen, Markus M MM; Molderings, Gerhard J GJ
Publication Date: 2012-11

Variant appearance in text: KIT: G286R
PubMed Link: 22957768
Variant Present in the following documents:
  • Main text
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