Allele Registry

Canonical Allele Identifier: PA645391520

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000486020

ClinVar Variation:

423597

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Ile4867Thr	CA16617111 NM_001035.3:c.14600T>C