Canonical Allele Identifier: PA2828361625
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1316357
ClinVar RCV Id: RCV001766263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Phe1874Ser
CA384889072
NM_001369788.1:c.5621T>C