SCN5A c.5275_5277delinsAAG ;(p.F1759K)

Variant ID: 3-38592583-GAA-CTT

NM_000335.4(SCN5A):c.5275_5277delinsAAG;(p.F1759K)

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:

New treatment options for late Na current, arrhythmias, and diastolic dysfunction.

Current Heart Failure Reports
Maier, Lars S LS
Publication Date: 2012-09

Variant appearance in text: SCN5A: F1759K
PubMed Link: 22767404
Variant Present in the following documents:
  • Main text
  • 11897_2012_Article_99.pdf
View BVdb publication page