Allele Registry

Canonical Allele Identifier: PA234851

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059405

RCV000723903

RCV001476333

RCV001836728

ClinVar Variation:

68532

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Glu1227Asp	CA234849 NM_006920.6:c.3681A>C CA349054671 NM_006920.6:c.3681A>T