Allele Registry

Canonical Allele Identifier: PA1139696231

Gene: RYR3 HGNC NCBI

ClinVar Variation Id: 977427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230925.1:p.Met1531Ile	CA7459050 NM_001243996.4:c.4593G>A CA391566842 NM_001243996.4:c.4593G>C CA391566843 NM_001243996.4:c.4593G>T