LIPC c.1100C>T ;(p.P367L)

Variant ID: 15-58853111-C-T

NM_000236.2(LIPC):c.1100C>T;(p.P367L)

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:

Genetics of Lipid and Lipoprotein Disorders and Traits.

Current Genetic Medicine Reports
Dron, Jacqueline S JS; Hegele, Robert A RA
Publication Date: 2016

Variant appearance in text: LIPC: P367L
PubMed Link: 28286704
Variant Present in the following documents:
  • Main text
  • 40142_2016_Article_97.pdf
View BVdb publication page