Canonical Allele Identifier: PA2825349014
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074229
ClinVar RCV Id: RCV004012771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Trp159Leu
CA345375421
NM_001035.3:c.476G>T