Canonical Allele Identifier: PA306891
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 201287
ClinVar RCV Id: RCV000182770 RCV001184236 RCV001192694 RCV002415776 RCV002515331 RCV003996768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Gly7Ser
CA008658
NM_001035.3:c.19G>A