Canonical Allele Identifier: PA915953601
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 665174
ClinVar RCV Id: RCV002535983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Ile4197Leu
CA345413693
NM_001035.3:c.12589A>C