Canonical Allele Identifier: PA2827786564
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Arg1620His
CA256584
NM_001353958.2:c.4859G>A