Canonical Allele Identifier: PA2827783828
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68567
ClinVar RCV Id: RCV000059442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Gly1734Glu
CA285012
NM_001353957.2:c.5201G>A