Allele Registry

Canonical Allele Identifier: PA2826010778

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001971003

ClinVar Variation:

1474062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Thr1658Ser	CA349069931 NM_001165963.4:c.4972A>T