Canonical Allele Identifier: PA2827292917
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1750018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Tyr1947Cys
CA384889830
NM_001330260.2:c.5840A>G