Canonical Allele Identifier: PA2499235663
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Met2389Leu
CA087313
NM_001035.3:c.7165A>C
CA345396681
NM_001035.3:c.7165A>T