Canonical Allele Identifier: PA2827758613
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Glu943Lys
CA285102
NM_001353949.2:c.2827G>A