Allele Registry

Canonical Allele Identifier: PA645390652

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000298794

RCV001093733

RCV001188871

RCV001582919

RCV001764262

RCV002450844

RCV003995825

ClinVar Variation:

296749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Glu3654Asp	CA084638 NM_001035.3:c.10962A>C CA345418951 NM_001035.3:c.10962A>T