Canonical Allele Identifier: PA105902
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133139
ClinVar RCV Id: RCV000119628 RCV001588950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Gly165Arg
CA024473
NM_000540.3:c.493G>A
CA405676912
NM_000540.3:c.493G>C