KCNH2 c.459del ;(p.W154Gfs*12)

Variant ID: 7-150656673-AG-A

NM_000238.3(KCNH2):c.459del;(p.W154Gfs*12)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.

Journal Of Medical Genetics
Lopes, Luis R LR; Zekavati, Anna A; Syrris, Petros P; Hubank, Mike M; Giambartolomei, Claudia C; Dalageorgou, Chrysoula C; Jenkins, Sharon S; McKenna, William W; , ; Plagnol, Vincent V; Elliott, Perry M PM
Publication Date: 2013-04

Variant appearance in text: KCNH2: 459delC
PubMed Link: 23396983
Variant Present in the following documents:
  • Main text
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