Allele Registry

Canonical Allele Identifier: PA645402993

Gene: SCN1A HGNC NCBI

ClinVar Variation Id: 418475

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Arg500Trp	CA1943296 NM_006920.6:c.1498C>T