Canonical Allele Identifier: PA913193210
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 628884
ClinVar RCV Id: RCV000773549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Val2111Ala
CA087092
NM_001035.3:c.6332T>C