SCN5A c.99C>T ;(p.A33=)

Variant ID: 3-38674700-G-A

NM_000335.4(SCN5A):c.99C>T;(p.A33=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Transcriptome alterations in myotonic dystrophy skeletal muscle and heart.

Human Molecular Genetics
Wang, Eric T ET; Treacy, Daniel D; Eichinger, Katy K; Struck, Adam A; Estabrook, Joseph J; Olafson, Hailey H; Wang, Thomas T TT; Bhatt, Kirti K; Westbrook, Tony T; Sedehizadeh, Sam S; Ward, Amanda A; Day, John J; Brook, David D; Berglund, J Andrew JA; Cooper, Thomas T; Housman, David D; Thornton, Charles C; Burge, Christopher C
Publication Date: 2019-04-15

Variant appearance in text: SCN5A: A33A
PubMed Link: 30561649
Variant Present in the following documents:
  • Main text
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