Canonical Allele Identifier: PA2825195827
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070685
ClinVar RCV Id: RCV004013195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Thr621Ser
CA405693978
NM_000540.3:c.1861A>T
CA405693984
NM_000540.3:c.1862C>G