Canonical Allele Identifier: PA105913
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133142
ClinVar RCV Id: RCV000119631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Gly1704Ser
CA024481
NM_000540.3:c.5110G>A