Allele Registry

Canonical Allele Identifier: PA132963

Gene: RYR2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000036729

RCV000157454

RCV000171762

RCV000769783

RCV000845327

RCV001098853

RCV001098854

RCV001254751

RCV001293091

RCV002453307

ClinVar Variation:

43769

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Glu1127Gly	CA009209 NM_001035.3:c.3380A>G