Canonical Allele Identifier: PA231933
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Phe4921Ser
CA024251
NM_000540.3:c.14762T>C