Canonical Allele Identifier: PA2580121239
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719486
ClinVar RCV Id: RCV003097960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Ser166Phe
CA345375506
NM_001035.3:c.497C>T