ALK c.837del ;(p.L280Cfs*55)

Variant ID: 2-29917831-GT-G

NM_004304.4(ALK):c.837del;(p.L280Cfs*55)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Development, Implementation and Assessment of Molecular Diagnostics by Next Generation Sequencing in Personalized Treatment of Cancer: Experience of a Public Reference Healthcare Hospital.

Cancers
Simarro, Javier J; Murria, Rosa R; Pérez-Simó, Gema G; Llop, Marta M; Mancheño, Nuria N; Ramos, David D; Juan, Inmaculada de I; Barragán, Eva E; Laiz, Begoña B; Cases, Enrique E; Ansótegui, Emilio E; Gómez-Codina, José J; Aparicio, Jorge J; Salvador, Carmen C; Juan, Óscar Ó; Palanca, Sarai S
Publication Date: 2019-08-16

Variant appearance in text: ALK: 837_837del
PubMed Link: 31426418
Variant Present in the following documents:
  • cancers-11-01196-s001.pdf
View BVdb publication page