MYL2 c.284C>G ;(p.P95R)

Variant ID: 12-111351119-G-C

NM_000432.3(MYL2):c.284C>G;(p.P95R)

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:

In the thick of it: HCM-causing mutations in myosin binding proteins of the thick filament.

Circulation Research
Harris, Samantha P SP; Lyons, Ross G RG; Bezold, Kristina L KL
Publication Date: 2011-03-18

Variant appearance in text: MYL2: P95R
PubMed Link: 21415409
Variant Present in the following documents:
  • Main text
View BVdb publication page