Canonical Allele Identifier: PA132960
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43767
ClinVar RCV Id: RCV000036726 RCV001191833 RCV002513414 RCV002444472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Val1077Ala
CA009141
NM_001035.3:c.3230T>C