Canonical Allele Identifier: PA107687
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68658
ClinVar RCV Id: RCV000059538 RCV001246264
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Gly177Glu
CA285231
NM_001165963.4:c.530G>A