Canonical Allele Identifier: PA2499277944
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1199237
ClinVar RCV Id: RCV001563669 RCV002570745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Glu290Lys
CA385226704
NM_014191.4:c.868G>A