Canonical Allele Identifier: PA346610
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 180488
ClinVar RCV Id: RCV000157447 RCV000590785 RCV002453531 RCV001191829 RCV003103738 RCV003998338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Gly797Arg
CA008789
NM_001035.3:c.2389G>A
CA345393391
NM_001035.3:c.2389G>C