Allele Registry

Canonical Allele Identifier: PA106961

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059536

RCV001062878

ClinVar Variation:

68656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ala175Thr	CA285225 NM_001165963.4:c.523G>A