Canonical Allele Identifier: PA2826260600
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Asp1804Asn
CA349067735
NM_001202435.3:c.5410G>A