Canonical Allele Identifier: PA2826010971
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1066554
ClinVar RCV Id: RCV001377574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Asp1742Asn
CA1942685
NM_001165963.4:c.5224G>A