SCN4A c.2620G>C ;(p.A874P)

Variant ID: 17-62029017-C-G

NM_000334.4(SCN4A):c.2620G>C;(p.A874P)

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: HYPP: A874P
PubMed Link: 28150151
Variant Present in the following documents:
  • Main text
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