Allele Registry

Canonical Allele Identifier: PA346617

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000157462

ClinVar Variation:

180499

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Gly3118Arg	CA011170 NM_001035.3:c.9352G>A CA345406236 NM_001035.3:c.9352G>C