Canonical Allele Identifier: PA284981
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Cys1577Arg
CA284979
NM_006920.6:c.4729T>C