Canonical Allele Identifier: PA2826013857
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1745814
ClinVar RCV Id: RCV002338406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly1697_Trp1698del
CA2580064420
NM_001165964.3:c.5090_5095del