Canonical Allele Identifier: PA2827750609
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1309815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Glu443Lys
CA349070496
NM_001353948.2:c.1327G>A