SCN5A c.706_708delinsATC ;(p.L236I)

Variant ID: 3-38651451-CAG-GAT

NM_000335.4(SCN5A):c.706_708delinsATC;(p.L236I)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.

Biomedical Reports
Golubenko, Maria M; Mikhailov, Vadim V; Rusinova, Valeria V; Shestak, Anna A; Zaklyazminskaya, Elena E
Publication Date: 2020-09

Variant appearance in text: SCN5A: Leu236Ile
PubMed Link: 32765855
Variant Present in the following documents:
  • Main text
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