PRRT2 c.621A>C ;(p.K207N)

Variant ID: 16-29824996-A-C

NM_145239.2(PRRT2):c.621A>C;(p.K207N)

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:

Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes.

Plos One
Lee, Cha Gon CG; Lee, Jeehun J; Lee, Munhyang M
Publication Date: 2018

Variant appearance in text: PRRT2: Lys207Asn
PubMed Link: 29924869
Variant Present in the following documents:
  • Main text
  • pone.0199321.pdf
View BVdb publication page