Canonical Allele Identifier: PA212049
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 224382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Pro1773Ser
CA066877
NM_000540.3:c.5317C>T