Allele Registry

Canonical Allele Identifier: PA645391061

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000478862

ClinVar Variation:

420865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Val4190Gly	CA16617110 NM_001035.3:c.12569T>G