Allele Registry

Canonical Allele Identifier: PA645390828

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000490203

RCV002523420

ClinVar Variation:

427164

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Met3972Val	CA345410102 NM_001035.3:c.11914A>G