Allele Registry

Canonical Allele Identifier: PA2827780130

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000474675

ClinVar Variation:

408922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Cys1342Phe	CA16610188 NM_001353955.2:c.4025G>T