Canonical Allele Identifier: PA2827790306
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gly136Glu
CA284913
NM_001353961.2:c.407G>A