Allele Registry

Canonical Allele Identifier: PA1139673896

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV002552507

ClinVar Variation:

840374

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Pro2328Ala	CA345395838 NM_001035.3:c.6982C>G