Canonical Allele Identifier: PA2827783495
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Gly1558Glu
CA285180
NM_001353957.2:c.4673G>A