Canonical Allele Identifier: PA2828361629
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1445246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Thr1879Pro
CA384889193
NM_001369788.1:c.5635A>C