SCN5A c.234G>C ;(p.E78D)

Variant ID: 3-38674565-C-G

NM_000335.4(SCN5A):c.234G>C;(p.E78D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Structure-based assessment of disease-related mutations in human voltage-gated sodium channels.

Protein & Cell
Huang, Weiyun W; Liu, Minhao M; Yan, S Frank SF; Yan, Nieng N
Publication Date: 2017-06

Variant appearance in text: LQT3: E78D
PubMed Link: 28150151
Variant Present in the following documents:
  • Main text
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