Canonical Allele Identifier: PA306917
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 155833
ClinVar RCV Id: RCV000143948 RCV000182797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Tyr3857Cys
CA007077
NM_001035.3:c.11570A>G