Canonical Allele Identifier: PA2827761478
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68567
ClinVar RCV Id: RCV000059442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Gly1751Glu
CA285012
NM_001353949.2:c.5252G>A