TTN c.2925_2926insCG ;(p.W976Rfs*17)

Variant ID: 2-179647707-A-ACG

NM_001267550.1(TTN):c.2925_2926insCG;(p.W976Rfs*17)

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:

Human Induced Pluripotent Stem Cells as a Platform for Personalized and Precision Cardiovascular Medicine.

Physiological Reviews
Matsa, Elena E; Ahrens, John H JH; Wu, Joseph C JC
Publication Date: 2016-07

Variant appearance in text: TTN: W976Rfs
PubMed Link: 27335446
Variant Present in the following documents:
  • Main text
View BVdb publication page