Variant ID: 1-55527143-G-C

NM_174936.3(PCSK9):c.1777G>C;(p.E593Q)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Shortcomings on genetic testing of Familial hypercholesterolemia (FH) in India: Can we collaborate to establish Indian FH Registry?

Indian Heart Journal
Reddy, Lakshmi Lavanya LL; Shah, Swarup A V SAV; Ashavaid, Tester F TF
Publication Date: 2021-12-04

Variant appearance in text: PCSK9: 1777G>C
PubMed Link: 34875256
Variant Present in the following documents:
  • main.pdf
View BVdb publication page