HNF4A c.593_594delinsAA ;(p.L198Q)

Variant ID: 20-43047075-TC-AA

NM_175914.4(HNF4A):c.593_594delinsAA;(p.L198Q)

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: HNF4A: L198Q
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page