Canonical Allele Identifier: PA645389293
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404210
ClinVar RCV Id: RCV000756606 RCV001099048 RCV000769785 RCV000852597 RCV000620181 RCV001099049 RCV004539926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Ser1765Cys
CA086866
NM_001035.3:c.5294C>G