Canonical Allele Identifier: PA2826010934
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1745814
ClinVar RCV Id: RCV002338406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Gly1725_Trp1726del
CA2580064420
NM_001165963.4:c.5174_5179del