MYH7 c.4135_4136delinsCG ;(p.A1379R)

Variant ID: 14-23887452-GC-CG

NM_000257.2(MYH7):c.4135_4136delinsCG;(p.A1379R)

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:

Genetics of inherited cardiomyopathies in Africa.

Cardiovascular Diagnosis And Therapy
Shaboodien, Gasnat G; Spracklen, Timothy F TF; Kamuli, Stephen S; Ndibangwi, Polycarp P; Van Niekerk, Carla C; Ntusi, Ntobeko A B NAB
Publication Date: 2020-04

Variant appearance in text: MYH7: A1379R
PubMed Link: 32420109
Variant Present in the following documents:
  • Main text
View BVdb publication page