SCN5A c.2908C>T ;(p.L970=)

Variant ID: 3-38622742-G-A

NM_000335.4(SCN5A):c.2908C>T;(p.L970=)

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:

Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies.

Cardiovascular Therapeutics
Amarouch, Mohamed-Yassine MY; El Hilaly, Jaouad J
Publication Date: 2020

Variant appearance in text: ICCD: 2908C>T
PubMed Link: 33381229
Variant Present in the following documents:
  • Main text
View BVdb publication page