Canonical Allele Identifier: PA346622
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180505
ClinVar RCV Id: RCV000157468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Ile4855Met
CA008301
NM_001035.3:c.14565T>G