Canonical Allele Identifier: PA2580370670
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2429008
ClinVar RCV Id: RCV003123249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ile1756Ser
CA384885081
NM_014191.4:c.5267T>G