Allele Registry

Canonical Allele Identifier: PA2827786587

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001971003

ClinVar Variation:

1474062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Thr1630Ser	CA349069931 NM_001353958.2:c.4888A>T