Canonical Allele Identifier: PA2826014000
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1523055
ClinVar RCV Id: RCV002048821
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp1776Asn
CA349067735
NM_001165964.3:c.5326G>A