Canonical Allele Identifier: PA306799
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 201192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Thr153Ile
CA009566
NM_001035.3:c.458C>T