Canonical Allele Identifier: PA2827784710
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Cys345Arg
CA303376
NM_001353958.2:c.1033T>C