Allele Registry

Canonical Allele Identifier: PA317664

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189019

RCV002517890

ClinVar Variation:

206880

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Ser1907Phe	CA317662 NM_006920.6:c.5720C>T