Canonical Allele Identifier: PA2580229667
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1721341
ClinVar RCV Id: RCV002300330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Phe409Val
CA349055876
NM_001353961.2:c.1225T>G