Canonical Allele Identifier: PA2827786200
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 954874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Lys1404Glu
CA349049625
NM_001353958.2:c.4210A>G