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FLNB c.1980C>A ;(p.C660*)
Variant ID: 3-58094223-C-A
NM_001457.3(
FLNB
):c.1980C>A;(p.C660*)
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:
Pharmacogenomics Variability of Lipid-Lowering Therapies in Familial Hypercholesterolemia.
Journal Of Personalized Medicine
Hindi, Nagham N NN; Alenbawi, Jamil J; Nemer, Georges G
Publication Date: 2021-08-31
Variant appearance in text: FH1: C660X
PubMed Link:
34575654
Variant Present in the following documents:
Main text
jpm-11-00877.pdf
View BVdb publication page