Canonical Allele Identifier: PA281913
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu975Phe
CA281911
NM_006920.6:c.2923C>T