SCN5A c.932del ;(p.P311Qfs*32)

Variant ID: 3-38651226-TG-T

NM_000335.4(SCN5A):c.932del;(p.P311Qfs*32)

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:

A contemporary review on the genetic basis of atrial fibrillation.

Methodist Debakey Cardiovascular Journal
Roberts, Jason D JD; Gollob, Michael H MH
Publication Date: 2014

Variant appearance in text: SCN5A: 932delC
PubMed Link: 24932358
Variant Present in the following documents:
  • Main text
View BVdb publication page