SCN5A c.799A>C ;(p.I267L)

Variant ID: 3-38651360-T-G

NM_000335.4(SCN5A):c.799A>C;(p.I267L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.

Mayo Clinic Proceedings
Tester, David J DJ; Medeiros-Domingo, Argelia A; Will, Melissa L ML; Haglund, Carla M CM; Ackerman, Michael J MJ
Publication Date: 2012-06

Variant appearance in text: SCN5A: I267L
PubMed Link: 22677073
Variant Present in the following documents:
  • Main text
View BVdb publication page