Canonical Allele Identifier: PA2826009259
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 283002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala420Asp
CA10604364
NM_001165963.4:c.1259C>A