Canonical Allele Identifier: PA2829675068
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 372741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Glu777Lys
CA16042443
NM_006920.6:c.2329G>A