Allele Registry

Canonical Allele Identifier: PA306852

Gene: RYR2 HGNC NCBI

ClinVar RCV:

RCV000143946

RCV000157455

RCV000182725

RCV000766716

RCV001186230

RCV002514771

RCV003998155

ClinVar Variation:

155831

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026.2:p.Met1564Ile	CA009643 NM_001035.3:c.4692G>A CA345402191 NM_001035.3:c.4692G>C CA345402193 NM_001035.3:c.4692G>T