Canonical Allele Identifier: PA2827758719
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Gly968Glu
CA303559
NM_001353949.2:c.2903G>A