APP c.866A>T ;(p.E289V)

Variant ID: 21-27372497-T-A

NM_000484.3(APP):c.866A>T;(p.E289V)

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:

Application of next-generation sequencing technologies in Neurology.

Annals Of Translational Medicine
Jiang, Teng T; Tan, Meng-Shan MS; Tan, Lan L; Yu, Jin-Tai JT
Publication Date: 2014-12

Variant appearance in text: APP: E289V
PubMed Link: 25568878
Variant Present in the following documents:
  • Main text
View BVdb publication page