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TTN c.66498dup ;(p.D22167*)
Variant ID: 2-179446496-C-CA
NM_001267550.1(
TTN
):c.66498dup;(p.D22167*)
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:
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome.
Heart Rhythm O2
Giudicessi, John R JR; Maleszewski, Joseph J JJ; Tester, David J DJ; Ackerman, Michael J MJ
Publication Date: 2021-10
Variant appearance in text: N/A
PubMed Link:
34667957
Variant Present in the following documents:
View BVdb publication page