APP c.960T>G ;(p.F320L)

Variant ID: 21-27372403-A-C

NM_000484.3(APP):c.960T>G;(p.F320L)

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:

A Comprehensive Analysis of the Role of hnRNP A1 Function and Dysfunction in the Pathogenesis of Neurodegenerative Disease.

Frontiers In Molecular Biosciences
Clarke, Joseph P JP; Thibault, Patricia A PA; Salapa, Hannah E HE; Levin, Michael C MC
Publication Date: 2021

Variant appearance in text: APP: F320L
PubMed Link: 33912591
Variant Present in the following documents:
  • Main text
View BVdb publication page