Canonical Allele Identifier: PA2825354654
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3069570
ClinVar RCV Id: RCV004008114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Thr2381Ala
CA345396597
NM_001035.3:c.7141A>G