Canonical Allele Identifier: PA2827783906
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Asp1776Asn
CA349067735
NM_001353957.2:c.5326G>A