Canonical Allele Identifier: PA2827786461
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Cys1560Arg
CA284979
NM_001353958.2:c.4678T>C