Canonical Allele Identifier: PA645389446
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377080

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Arg2100Gln
CA16603260
NM_001035.3:c.6299G>A