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KCNH2 c.1759C>G ;(p.H587D)
Variant ID: 7-150648722-G-C
NM_000238.3(
KCNH2
):c.1759C>G;(p.H587D)
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:
Effect of S5P alpha-helix charge mutants on inactivation of hERG K+ channels.
The Journal Of Physiology
Clarke, C E CE; Hill, A P AP; Zhao, J J; Kondo, M M; Subbiah, R N RN; Campbell, T J TJ; Vandenberg, J I JI
Publication Date: 2006-06-01
Variant appearance in text: HERG: H587D
PubMed Link:
16556651
Variant Present in the following documents:
Main text
View BVdb publication page