Canonical Allele Identifier: PA916036872
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Cys774Arg
CA284979
NM_001353961.2:c.2320T>C