PRRT2 c.637G>C ;(p.G213R)

Variant ID: 16-29825012-G-C

NM_145239.2(PRRT2):c.637G>C;(p.G213R)

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:

Targeting Tau to Treat Clinical Features of Huntington's Disease.

Frontiers In Neurology
Masnata, Maria M; Salem, Shireen S; de Rus Jacquet, Aurelie A; Anwer, Mehwish M; Cicchetti, Francesca F
Publication Date: 2020

Variant appearance in text: PKC: G213R
PubMed Link: 33329322
Variant Present in the following documents:
  • Main text
  • fneur-11-580732.pdf
View BVdb publication page