Canonical Allele Identifier: PA913192843
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 618352
ClinVar RCV Id: RCV000756608 RCV001179696 RCV002533793 RCV003999887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Arg272His
CA345383698
NM_001035.3:c.815G>A