Canonical Allele Identifier: PA285182
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly1575Glu
CA285180
NM_006920.6:c.4724G>A