Canonical Allele Identifier: PA2826008795
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2050782
ClinVar RCV Id: RCV002904618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Asn86His
CA349242637
NM_001165963.4:c.256A>C