Canonical Allele Identifier: PA2826011182
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1748495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Cys1864Ser
CA349065298
NM_001165963.4:c.5591G>C
CA349065313
NM_001165963.4:c.5590T>A