MYH7 c.1426C>T ;(p.L476F)

Variant ID: 14-23897861-G-A

NM_000257.2(MYH7):c.1426C>T;(p.L476F)

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:

Genotype-Related Clinical Characteristics and Myocardial Fibrosis and their Association with Prognosis in Hypertrophic Cardiomyopathy.

Journal Of Clinical Medicine
Kim, Hyung Yoon HY; Park, Jong Eun JE; Lee, Sang-Chol SC; Jeon, Eun-Seok ES; On, Young Keun YK; Kim, Sung Mok SM; Choe, Yeon Hyeon YH; Ki, Chang-Seok CS; Kim, Jong-Won JW; Kim, Kye Hun KH
Publication Date: 2020-06-01

Variant appearance in text: MYH7: 1426C>T; Leu476Phe
PubMed Link: 32492895
Variant Present in the following documents:
  • Main text
  • jcm-09-01671.pdf
View BVdb publication page