Canonical Allele Identifier: PA2827767857
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1745814
ClinVar RCV Id: RCV002338406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Gly1714_Trp1715del
CA2580064420
NM_001353950.2:c.5141_5146del