Allele Registry

Canonical Allele Identifier: PA2827787034

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189019

RCV002517890

ClinVar Variation:

206880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Ser1890Phe	CA317662 NM_001353958.2:c.5669C>T