Variant ID: 1-55505646-C-T

NM_174936.3(PCSK9):c.136C>T;(p.R46C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pharmacogenomics Variability of Lipid-Lowering Therapies in Familial Hypercholesterolemia.

Journal Of Personalized Medicine
Hindi, Nagham N NN; Alenbawi, Jamil J; Nemer, Georges G
Publication Date: 2021-08-31

Variant appearance in text: PCSK9: 136C>T
PubMed Link: 34575654
Variant Present in the following documents:
  • Main text
  • jpm-11-00877.pdf
View BVdb publication page