Allele Registry

Canonical Allele Identifier: PA916036372

Gene: SCN1A HGNC NCBI

ClinVar Variation Id: 189929

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Pro768Leu	CA303333 NM_001353948.2:c.2303C>T