Canonical Allele Identifier: PA2826013589
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly1558Glu
CA285180
NM_001165964.3:c.4673G>A