Canonical Allele Identifier: PA645449525
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 374665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.His1727Gln
CA16043838
NM_014191.4:c.5181C>A
CA384884291
NM_014191.4:c.5181C>G