Canonical Allele Identifier: PA209899
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Arg885His
CA063661
NM_000540.3:c.2654G>A