Canonical Allele Identifier: PA266128
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68660
ClinVar RCV Id: RCV000059540 RCV000489760 RCV000764284 RCV000792317
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Glu1784Lys
CA266126
NM_006920.6:c.5350G>A