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ALK c.977_978delinsGT ;(p.S326C)
Variant ID: 2-29754957-TG-AC
NM_004304.4(
ALK
):c.977_978delinsGT;(p.S326C)
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:
Functional Polymorphisms in hOGG1 Gene and Neuroblastoma Risk in Chinese Children.
Journal Of Cancer
Wang, Yi-Zhen YZ; Zhuo, Zhen-Jian ZJ; Fang, Yuan Y; Li, Lin L; Zhang, Jiao J; He, Jing J; Wu, Xue-Mei XM
Publication Date: 2018
Variant appearance in text: ALK: Ser326Cys
PubMed Link:
30519358
Variant Present in the following documents:
Main text
jcav09p4521.pdf
View BVdb publication page