Canonical Allele Identifier: PA2827766187
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Leu1276Pro
CA285150
NM_001353950.2:c.3827T>C