ALK c.1180_1182delinsAGC ;(p.G394S)

Variant ID: 2-29606698-CCC-GCT

NM_004304.4(ALK):c.1180_1182delinsAGC;(p.G394S)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

The Conundrum of Genetic "Drivers" in Benign Conditions.

Journal Of The National Cancer Institute
Kato, Shumei S; Lippman, Scott M SM; Flaherty, Keith T KT; Kurzrock, Razelle R
Publication Date: 2016-08

Variant appearance in text: ALK: G394S
PubMed Link: 27059373
Variant Present in the following documents:
  • Main text
  • djw036.pdf
View BVdb publication page