Canonical Allele Identifier: PA2827754242
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Val1612Ile
CA285183
NM_001353948.2:c.4834G>A