APOB c.1824C>T ;(p.I608=)

Variant ID: 2-21251204-G-A

NM_000384.2(APOB):c.1824C>T;(p.I608=)

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:

Gene Therapy for Cardiovascular Disease: Basic Research and Clinical Prospects.

Frontiers In Cardiovascular Medicine
Cao, Genmao G; Xuan, Xuezhen X; Zhang, Ruijing R; Hu, Jie J; Dong, Honglin H
Publication Date: 2021

Variant appearance in text: APOB: 1824C>T
PubMed Link: 34805315
Variant Present in the following documents:
  • Main text
  • fcvm-08-760140.pdf
View BVdb publication page