Canonical Allele Identifier: PA2827790287
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 381569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ser126Phe
CA16604035
NM_001353961.2:c.377C>T