Allele Registry

Canonical Allele Identifier: PA346624

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000157470

ClinVar Variation:

180507

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Thr4909Ile	CA008359 NM_001035.3:c.14726C>T