Canonical Allele Identifier: PA2580230210
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1745814
ClinVar RCV Id: RCV002338406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gly911_Trp912del
CA2580064420
NM_001353961.2:c.2732_2737del