Allele Registry

Canonical Allele Identifier: PA2827774157

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000474675

ClinVar Variation:

408922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Cys1343Phe	CA16610188 NM_001353952.2:c.4028G>T