APP c.188T>C ;(p.I63T)

Variant ID: 21-27484333-A-G

NM_000484.3(APP):c.188T>C;(p.I63T)

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:

Nigral iron elevation is an invariable feature of Parkinson's disease and is a sufficient cause of neurodegeneration.

Biomed Research International
Ayton, Scott S; Lei, Peng P
Publication Date: 2014

Variant appearance in text: APP: I63T
PubMed Link: 24527451
Variant Present in the following documents:
  • Main text
View BVdb publication page