Canonical Allele Identifier: PA2827762553
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 567303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ala104Asp
CA349077094
NM_001353950.2:c.311C>A