Canonical Allele Identifier: PA645389461
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 404214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Thr2116Ala
CA087095
NM_001035.3:c.6346A>G