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SCN5A c.393G>C ;(p.S131=)
Variant ID: 3-38663980-C-G
NM_000335.4(
SCN5A
):c.393G>C;(p.S131=)
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:
Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies.
Cardiovascular Therapeutics
Amarouch, Mohamed-Yassine MY; El Hilaly, Jaouad J
Publication Date: 2020
Variant appearance in text: PFHB1: 393G>C
PubMed Link:
33381229
Variant Present in the following documents:
Main text
View BVdb publication page