Canonical Allele Identifier: PA2828361642
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1411036
ClinVar RCV Id: RCV001920417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Lys1893Glu
CA384889514
NM_001369788.1:c.5677A>G