Canonical Allele Identifier: PA2827767303
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Cys1577Arg
CA284979
NM_001353950.2:c.4729T>C