Canonical Allele Identifier: PA2827784431
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Gly177Glu
CA285231
NM_001353958.2:c.530G>A