Canonical Allele Identifier: PA2826011082
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Asp1804Asn
CA349067735
NM_001165963.4:c.5410G>A