RYR1 c.5339C>G ;(p.P1780R)

Variant ID: 19-38976634-C-G

NM_000540.2(RYR1):c.5339C>G;(p.P1780R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical pharmacogenetic analysis in 5,001 individuals with diagnostic Exome Sequencing data.

Npj Genomic Medicine
Lanillos, Javier J; Carcajona, Marta M; Maietta, Paolo P; Alvarez, Sara S; Rodriguez-Antona, Cristina C
Publication Date: 2022-02-18

Variant appearance in text: RYR1: 5339C>G; Pro1780Arg; rs369480385
PubMed Link: 35181665
Variant Present in the following documents:
  • 41525_2022_283_MOESM4_ESM.xlsx, sheet 1
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