SCN5A c.4880C>G ;(p.A1627G)

Variant ID: 3-38592980-G-C

NM_000335.4(SCN5A):c.4880C>G;(p.A1627G)

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:

Screening for 392 polymorphisms in 141 pharmacogenes.

Biomedical Reports
Kim, Jason Yongha JY; Cheong, Hyun Sub HS; Park, Tae-Joon TJ; Shin, Hee Jung HJ; Seo, Doo Won DW; Na, Han Sung HS; Chung, Myeon Woo MW; Shin, Hyoung Doo HD
Publication Date: 2014-07

Variant appearance in text: SCN5A: A1627G
PubMed Link: 24944790
Variant Present in the following documents:
  • Main text
View BVdb publication page