Allele Registry

Canonical Allele Identifier: PA306923

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000182804

RCV002515334

ClinVar Variation:

201319

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Asn3989Asp	CA007278 NM_001035.3:c.11965A>G