SCN1A c.5929A>C ;(p.M1977L)

Variant ID: 2-166847856-T-G

NM_001165963.1(SCN1A):c.5929A>C;(p.M1977L)

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:

SCN1A Mutation-Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis.

Frontiers In Neurology
Ding, Jiangwei J; Li, Xinxiao X; Tian, Haiyan H; Wang, Lei L; Guo, Baorui B; Wang, Yangyang Y; Li, Wenchao W; Wang, Feng F; Sun, Tao T
Publication Date: 2021

Variant appearance in text: SCN1A: M1977L
PubMed Link: 35002916
Variant Present in the following documents:
  • Main text
  • fneur-12-743726.pdf
View BVdb publication page