Canonical Allele Identifier: PA916011881
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 691260
ClinVar RCV Id: RCV000851502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ala420Pro
CA385228163
NM_014191.4:c.1258G>C