Allele Registry

Canonical Allele Identifier: PA3057314663

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV004805467

ClinVar Variation:

3385702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Arg1084Met	CA345397957 NM_001035.3:c.3251G>T