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SCN5A c.4132A>C ;(p.N1378H)
Variant ID: 3-38601748-T-G
NM_000335.4(
SCN5A
):c.4132A>C;(p.N1378H)
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:
Structure-based assessment of disease-related mutations in human voltage-gated sodium channels.
Protein & Cell
Huang, Weiyun W; Liu, Minhao M; Yan, S Frank SF; Yan, Nieng N
Publication Date: 2017-06
Variant appearance in text: LQT3: N1378H
PubMed Link:
28150151
Variant Present in the following documents:
Main text
View BVdb publication page