Canonical Allele Identifier: PA106451
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 66004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Tyr4864Cys
CA024196
NM_000540.3:c.14591A>G