MYH7 c.1922G>A ;(p.G641D)

Variant ID: 14-23896483-C-T

NM_000257.2(MYH7):c.1922G>A;(p.G641D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy.

Basic Research In Cardiology
Tripathi, Snigdha S; Schultz, Imke I; Becker, Edgar E; Montag, Judith J; Borchert, Bianca B; Francino, Antonio A; Navarro-Lopez, Francisco F; Perrot, Andreas A; Özcelik, Cemil C; Osterziel, Karl-Josef KJ; McKenna, William J WJ; Brenner, Bernhard B; Kraft, Theresia T
Publication Date: 2011-11

Variant appearance in text: MYH7: 1922G>A
PubMed Link: 21769673
Variant Present in the following documents:
  • Main text
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