SCN5A c.4513C>T ;(p.P1505S)

Variant ID: 3-38597173-G-A

NM_000335.4(SCN5A):c.4513C>T;(p.P1505S)

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:

Complex genetic background in a large family with Brugada syndrome.

Physiological Reports
Saber, Siamak S; Amarouch, Mohamed-Yassine MY; Fazelifar, Amir-Farjam AF; Haghjoo, Majid M; Emkanjoo, Zahra Z; Alizadeh, Abolfath A; Houshmand, Massoud M; Gavrilenko, Alexander V AV; Abriel, Hugues H; Zaklyazminskaya, Elena V EV
Publication Date: 2015-01-01

Variant appearance in text: SCN5A: P1505S
PubMed Link: 25626866
Variant Present in the following documents:
  • Main text
  • phy2-3-e12256.pdf
View BVdb publication page