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KCNH2 c.778G>C ;(p.A260P)
Variant ID: 7-150655285-C-G
NM_000238.3(
KCNH2
):c.778G>C;(p.A260P)
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:
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.
European Journal Of Human Genetics : Ejhg
Robyns, Tomas T; Kuiperi, Cuno C; Breckpot, Jeroen J; Devriendt, Koenraad K; Souche, Erika E; Van Cleemput, Johan J; Willems, Rik R; Nuyens, Dieter D; Matthijs, Gert G; Corveleyn, Anniek A
Publication Date: 2017-12
Variant appearance in text: KCNH2: 778G>C
PubMed Link:
29255176
Variant Present in the following documents:
Main text
View BVdb publication page