Allele Registry

Canonical Allele Identifier: PA2826013722

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001971003

ClinVar Variation:

1474062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Thr1630Ser	CA349069931 NM_001165964.3:c.4888A>T