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PCSK9 c.1331T>C ;(p.L444P)
Variant ID: 1-55523859-T-C
NM_174936.3(
PCSK9
):c.1331T>C;(p.L444P)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic outline of the hermeneutics of the diseases connection phenomenon in human.
Vavilovskii Zhurnal Genetiki I Selektsii
Bragina, E Yu EY; Puzyrev, V P VP
Publication Date: 2023-03
Variant appearance in text: PCSK9: L444P
PubMed Link:
36923482
Variant Present in the following documents:
Main text
View BVdb publication page
The Resurrection of Phenotypic Drug Discovery.
Acs Medicinal Chemistry Letters
Childers, Wayne E WE; Elokely, Khaled M KM; Abou-Gharbia, Magid M
Publication Date: 2020-10-08
Variant appearance in text: PCSK9: L444P
PubMed Link:
33062159
Variant Present in the following documents:
Main text
View BVdb publication page