APP c.1832G>C ;(p.G611A)

Variant ID: 21-27284130-C-G

NM_000484.3(APP):c.1832G>C;(p.G611A)

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:

Mitochondrial genome changes and neurodegenerative diseases.

Biochimica Et Biophysica Acta
Pinto, Milena M; Moraes, Carlos T CT
Publication Date: 2014-08

Variant appearance in text: APP: G611A
PubMed Link: 24252612
Variant Present in the following documents:
  • Main text
View BVdb publication page