Variant ID: 1-55512243-CTT-C

NM_174936.3(PCSK9):c.449_450del;(p.F150Cfs*20)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.

European Journal Of Human Genetics : Ejhg
Brænne, Ingrid I; Kleinecke, Mariana M; Reiz, Benedikt B; Graf, Elisabeth E; Strom, Tim T; Wieland, Thomas T; Fischer, Marcus M; Kessler, Thorsten T; Hengstenberg, Christian C; Meitinger, Thomas T; Erdmann, Jeanette J; Schunkert, Heribert H
Publication Date: 2016-02

Variant appearance in text: PCSK9: 449_450del
PubMed Link: 26036859
Variant Present in the following documents:
  • Main text
View BVdb publication page