MYH7 c.962C>T ;(p.A321V)

Variant ID: 14-23899806-G-A

NM_000257.2(MYH7):c.962C>T;(p.A321V)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Impact of systolic dysfunction in genotyped hypertrophic cardiomyopathy.

Clinical Cardiology
Fujino, Noboru N; Konno, Tetsuo T; Hayashi, Kenshi K; Hodatsu, Akihiko A; Fujita, Takashi T; Tsuda, Toyonobu T; Nagata, Yoji Y; Kawashiri, Masa-aki MA; Ino, Hidekazu H; Yamagishi, Masakazu M
Publication Date: 2013-03

Variant appearance in text: MYH7: Ala321Val
PubMed Link: 23197398
Variant Present in the following documents:
  • Main text
View BVdb publication page