Canonical Allele Identifier: PA2827776946
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2581808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Gly1221Ser
CA349055647
NM_001353954.2:c.3661G>A