Canonical Allele Identifier: PA2827781868
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Val406Phe
CA248047
NM_001353957.2:c.1216G>T