Canonical Allele Identifier: PA2829676538
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asp1793Asn
CA349067735
NM_006920.6:c.5377G>A