TTN c.2596C>G ;(p.P866A)

Variant ID: 2-179648976-G-C

NM_001267550.1(TTN):c.2596C>G;(p.P866A)

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:

Sphingolipid abnormalities in cancer multidrug resistance: Chicken or egg?

Cellular Signalling
Lee, Wing-Kee WK; Kolesnick, Richard N RN
Publication Date: 2017-10

Variant appearance in text: TMD: P866A
PubMed Link: 28687494
Variant Present in the following documents:
  • Main text
View BVdb publication page