Canonical Allele Identifier: PA2828361527
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 941314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ile1786Thr
CA384886661
NM_001369788.1:c.5357T>C