Canonical Allele Identifier: PA306882
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 201278
ClinVar RCV Id: RCV000182759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Asp2397Tyr
CA010599
NM_001035.3:c.7189G>T