Canonical Allele Identifier: PA2827767297
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Gly1575Glu
CA285180
NM_001353950.2:c.4724G>A