SCN5A c.3161C>A ;(p.S1054*)

Variant ID: 3-38622489-G-T

NM_000335.4(SCN5A):c.3161C>A;(p.S1054*)

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:

Genetic Discovery of ATP-Sensitive K+ Channels in Cardiovascular Diseases.

Circulation. Arrhythmia And Electrophysiology
Huang, Yan Y; Hu, Dan D; Huang, Congxin C; Nichols, Colin G CG
Publication Date: 2019-05

Variant appearance in text: ICCD: 3161C>A
PubMed Link: 31030551
Variant Present in the following documents:
  • Main text
View BVdb publication page