Canonical Allele Identifier: PA2827780934
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Asp1792Asn
CA349067735
NM_001353955.2:c.5374G>A