Allele Registry

Canonical Allele Identifier: PA306931

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000182815

RCV001332695

ClinVar Variation:

201329

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Leu4101Phe	CA007454 NM_001035.3:c.12301C>T