Canonical Allele Identifier: PA2827771958
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Glu1784Lys
CA266126
NM_001353951.2:c.5350G>A