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PCSK9 c.418G>T ;(p.V140F)
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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
fgene-11-572045.pdf
View BVdb publication page