Allele Registry

Canonical Allele Identifier: PA266088

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059374

RCV000180936

RCV000188861

RCV001226020

RCV001775078

ClinVar Variation:

68502

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Arg377Gln	CA266086 NM_006920.6:c.1130G>A