Canonical Allele Identifier: PA303420
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Cys336Tyr
CA303417
NM_006920.6:c.1007G>A