Allele Registry

Canonical Allele Identifier: PA306970

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000182859

RCV001179067

RCV002516904

RCV003996791

RCV004020197

ClinVar Variation:

201370

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Ala266Thr	CA010816 NM_001035.3:c.796G>A