DMD c.826C>A ;(p.Q276K)

Variant ID: X-32717234-G-T

NM_004006.2(DMD):c.826C>A;(p.Q276K)

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:

Late-onset myopathies: clinical features and diagnosis.

Acta Myologica : Myopathies And Cardiomyopathies : Official Journal Of The Mediterranean Society Of Myology
de Visser, Marianne M
Publication Date: 2020-12

Variant appearance in text: DMD: 826C>A
PubMed Link: 33458579
Variant Present in the following documents:
  • Main text
  • am-2020-04-235.pdf
View BVdb publication page