PCSK9 c.1331T>C ;(p.L444P)

Variant ID: 1-55523859-T-C

NM_174936.3(PCSK9):c.1331T>C;(p.L444P)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic outline of the hermeneutics of the diseases connection phenomenon in human.

Vavilovskii Zhurnal Genetiki I Selektsii
Bragina, E Yu EY; Puzyrev, V P VP
Publication Date: 2023-03

Variant appearance in text: PCSK9: L444P
PubMed Link: 36923482
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Resurrection of Phenotypic Drug Discovery.

Acs Medicinal Chemistry Letters
Childers, Wayne E WE; Elokely, Khaled M KM; Abou-Gharbia, Magid M
Publication Date: 2020-10-08

Variant appearance in text: PCSK9: L444P
PubMed Link: 33062159
Variant Present in the following documents:
  • Main text
View BVdb publication page