Allele Registry

Canonical Allele Identifier: PA132951

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000036714

RCV000157446

RCV000242970

RCV000287643

RCV000786207

RCV001093912

RCV001181067

ClinVar Variation:

36739

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Ser756Asn	CA008736 NM_001035.3:c.2267G>A