Allele Registry

Canonical Allele Identifier: PA285152

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059502

RCV001385513

ClinVar Variation:

68624

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Leu1276Pro	CA285150 NM_006920.6:c.3827T>C