Variant ID: 1-55512214-G-T

NM_174936.3(PCSK9):c.418G>T;(p.V140F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype-Phenotype Correlations of the Disease.

Frontiers In Genetics
Kamar, Amina A; Khalil, Athar A; Nemer, Georges G
Publication Date: 2020

Variant appearance in text: PCSK9: 418G>T
PubMed Link: 33519890
Variant Present in the following documents:
  • Main text
View BVdb publication page