Canonical Allele Identifier: PA658659845
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Arg1988Gln
CA1942622
NM_001165963.4:c.5963G>A