Allele Registry

Canonical Allele Identifier: PA306966

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000182855

RCV001177416

RCV002390466

RCV003153463

RCV003996789

ClinVar Variation:

201366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Tyr4962Asn	CA008458 NM_001035.3:c.14884T>A