MYH7 c.4865T>C ;(p.L1622P)

Variant ID: 14-23885301-A-G

NM_000257.2(MYH7):c.4865T>C;(p.L1622P)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes.

Ebiomedicine
Campuzano, Oscar O; Sarquella-Brugada, Georgia G; Fernandez-Falgueras, Anna A; Coll, Mónica M; Iglesias, Anna A; Ferrer-Costa, Carles C; Cesar, Sergi S; Arbelo, Elena E; García-Álvarez, Ana A; Jordà, Paloma P; Toro, Rocío R; Tiron de Llano, Coloma C; Grassi, Simone S; Oliva, Antonio A; Brugada, Josep J; Brugada, Ramon R
Publication Date: 2020-04

Variant appearance in text: MYH7: 4865T>C; Leu1622Pro
PubMed Link: 32268277
Variant Present in the following documents:
  • Main text
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