Variant ID: 1-55523143-T-C

NM_174936.3(PCSK9):c.1136T>C;(p.F379S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Proceedings of the 24th Annual Meeting of the Portuguese Society of Human Genetics (SPGH - Sociedade Portuguesa de Genética Humana).

Medicine
Publication Date: 2021-01-29

Variant appearance in text: PCSK9: Phe379Ser
PubMed Link: 33530161
Variant Present in the following documents:
  • Main text
  • medi-100-e23585.pdf
View BVdb publication page