Canonical Allele Identifier: PA915965902
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Arg272Cys
CA087572
NM_001035.3:c.814C>T