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SCN5A c.2162T>C ;(p.L721P)
Variant ID: 3-38639320-A-G
NM_000335.4(
SCN5A
):c.2162T>C;(p.L721P)
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:
Etiology of sudden death in the community: results of anatomical, metabolic, and genetic evaluation.
American Heart Journal
Adabag, A Selcuk AS; Peterson, Garry G; Apple, Fred S FS; Titus, Jack J; King, Richard R; Luepker, Russell V RV
Publication Date: 2010-01
Variant appearance in text: SCN5A: L721P
PubMed Link:
20102864
Variant Present in the following documents:
Main text
View BVdb publication page