Canonical Allele Identifier: PA2826130858
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1750018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Tyr1906Cys
CA384889830
NM_001177984.2:c.5717A>G