Canonical Allele Identifier: PA2827768175
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Asp1793Asn
CA349067735
NM_001353950.2:c.5377G>A