KIT c.1847C>A ;(p.A616E)

Variant ID: 4-55594061-C-A

NM_000222.2(KIT):c.1847C>A;(p.A616E)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: KIT: A616E
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page