Canonical Allele Identifier: PA2827781768
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Asn359Ser
CA303143
NM_001353957.2:c.1076A>G