Canonical Allele Identifier: PA916012061
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 828188
ClinVar RCV Id: RCV001028097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ala1099Thr
CA384893484
NM_014191.4:c.3295G>A