Canonical Allele Identifier: PA211771
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Asp708Asn
CA024331
NM_000540.3:c.2122G>A