Allele Registry

Canonical Allele Identifier: PA306985

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000182878

RCV001175682

RCV002408798

RCV002516911

ClinVar Variation:

201388

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Asp2735Glu	CA010879 NM_001035.3:c.8205C>A CA345401283 NM_001035.3:c.8205C>G