Canonical Allele Identifier: PA2826013334
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 954874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Lys1404Glu
CA349049625
NM_001165964.3:c.4210A>G