Canonical Allele Identifier: PA916047890
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 748133
ClinVar RCV Id: RCV000924907 RCV001399312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg223Thr
CA385224699
NM_001369788.1:c.668G>C