PRRT2 c.56A>G ;(p.K19R)

Variant ID: 16-29824431-A-G

NM_145239.2(PRRT2):c.56A>G;(p.K19R)

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:

Ubiquitylation and endocytosis of the human LAT1/SLC7A5 amino acid transporter.

Scientific Reports
Barthelemy, Céline C; André, Bruno B
Publication Date: 2019-11-14

Variant appearance in text: PKC: K19R
PubMed Link: 31728037
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_53065.pdf
View BVdb publication page