Canonical Allele Identifier: PA913192991
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 629548
ClinVar RCV Id: RCV000774257 RCV002534126 RCV004001374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Arg1089His
CA086345
NM_001035.3:c.3266G>A