Canonical Allele Identifier: PA204278
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207949
ClinVar RCV Id: RCV000190227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Ser166Cys
CA204277
NM_001035.3:c.497C>G