MYH7 c.2150A>T ;(p.D717V)

Variant ID: 14-23895185-T-A

NM_000257.2(MYH7):c.2150A>T;(p.D717V)

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:

Perspectives on current recommendations for genetic testing in HCM.

Global Cardiology Science & Practice
Monserrat, Lorenzo L
Publication Date: 2018-08-12

Variant appearance in text: MYH7: Asp717Val
PubMed Link: 30393635
Variant Present in the following documents:
  • Main text
  • gcsp-2018-3-e201823.pdf
View BVdb publication page