Canonical Allele Identifier: PA658801613
Gene: RYR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 487620
ClinVar RCV Id: RCV000656197 RCV001176899 RCV002506386 RCV002367975 RCV003153749 RCV004001213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026.2:p.Pro1256Leu
CA086441
NM_001035.3:c.3767C>T