TTN c.96320G>A ;(p.G32107D)

Variant ID: 2-179408380-C-T

NM_001267550.1(TTN):c.96320G>A;(p.G32107D)

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:

Absence of a primary role for TTN missense variants in arrhythmogenic cardiomyopathy: From a clinical and pathological perspective.

Clinical Cardiology
Chen, Kai K; Song, Jiangping J; Wang, Zhen Z; Rao, Man M; Chen, Liang L; Hu, Shengshou S
Publication Date: 2018-05

Variant appearance in text: TTN: 96320G>A
PubMed Link: 29750433
Variant Present in the following documents:
  • Main text
View BVdb publication page