Allele Registry

Canonical Allele Identifier: PA2826259802

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000474675

ClinVar Variation:

408922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Cys1354Phe	CA16610188 NM_001202435.3:c.4061G>T