Allele Registry

Canonical Allele Identifier: PA645402616

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000481626

ClinVar Variation:

418590

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Leu170Pro	CA16617316 NM_006920.6:c.509T>C