Canonical Allele Identifier: PA2827784692
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Cys336Tyr
CA303417
NM_001353958.2:c.1007G>A