MYH7 c.598G>C ;(p.A200P)

Variant ID: 14-23901011-C-G

NM_000257.2(MYH7):c.598G>C;(p.A200P)

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:

Analysis of Contractile Function of Permeabilized Human Hypertrophic Cardiomyopathy Multicellular Heart Tissue.

Frontiers In Physiology
Kresin, Nico N; Stücker, Sabrina S; Krämer, Elisabeth E; Flenner, Frederik F; Mearini, Giulia G; Münch, Julia J; Patten, Monica M; Redwood, Charles C; Carrier, Lucie L; Friedrich, Felix W FW
Publication Date: 2019

Variant appearance in text: MYH7: 598G>C; Ala200Pro
PubMed Link: 30984009
Variant Present in the following documents:
  • Main text
  • fphys-10-00239.pdf
View BVdb publication page