MYBPC3 c.2671_2672delinsGC ;(p.R891A)

Variant ID: 11-47357493-CG-GC

NM_000256.3(MYBPC3):c.2671_2672delinsGC;(p.R891A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.

Frontiers In Genetics
Campuzano, Oscar O; Fernandez-Falgueras, Anna A; Sarquella-Brugada, Georgia G; Cesar, Sergi S; Arbelo, Elena E; García-Álvarez, Ana A; Jordà, Paloma P; Coll, Monica M; Fiol, Victoria V; Iglesias, Anna A; Perez-Serra, Alexandra A; Mates, Jesus J; Del Olmo, Bernat B; Ferrer, Carles C; Alcalde, Mireia M; Puigmulé, Marta M; Mademont-Soler, Irene I; Pico, Ferran F; Lopez, Laura L; Tiron, Coloma C; Brugada, Josep J; Brugada, Ramon R
Publication Date: 2019

Variant appearance in text: MYBPC3: R891A
PubMed Link: 31156706
Variant Present in the following documents:
  • Main text
  • fgene-10-00450.pdf
View BVdb publication page