APP c.797_798inv ;(p.T266M)

Variant ID: 21-27394223-TG-CA

NM_000484.3(APP):c.797_798inv;(p.T266M)

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:

Role of PITRM1 in Mitochondrial Dysfunction and Neurodegeneration.

Biomedicines
Brunetti, Dario D; Catania, Alessia A; Viscomi, Carlo C; Deleidi, Michela M; Bindoff, Laurence A LA; Ghezzi, Daniele D; Zeviani, Massimo M
Publication Date: 2021-07-17

Variant appearance in text: APP: T266M
PubMed Link: 34356897
Variant Present in the following documents:
  • Main text
  • biomedicines-09-00833.pdf
View BVdb publication page