Allele Registry

Canonical Allele Identifier: PA346622

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000157468

ClinVar Variation:

180505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Ile4855Met	CA008301 NM_001035.3:c.14565T>G