Allele Registry

Canonical Allele Identifier: PA645404224

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000474675

ClinVar Variation:

408922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Cys1354Phe	CA16610188 NM_001165963.4:c.4061G>T