Variant ID: 1-55529132-A-G

NM_174936.3(PCSK9):c.1954A>G;(p.N652D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction.

Lipids In Health And Disease
Lee, Chongyou C; Cui, Yuxia Y; Song, Junxian J; Li, Sufang S; Zhang, Feng F; Wu, Manyan M; Li, Long L; Hu, Dan D; Chen, Hong H
Publication Date: 2019-04-11

Variant appearance in text: PCSK9: 1954A>G; Asn652Asp
PubMed Link: 30971288
Variant Present in the following documents:
  • Main text
View BVdb publication page