Allele Registry

Canonical Allele Identifier: PA132962

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000036728

RCV000171761

RCV000234976

RCV000620350

RCV000656971

RCV000771794

RCV004541106

ClinVar Variation:

43768

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Thr1107Met	CA009188 NM_001035.3:c.3320C>T