Allele Registry

Canonical Allele Identifier: PA2827767581

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001971003

ClinVar Variation:

1474062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Thr1647Ser	CA349069931 NM_001353950.2:c.4939A>T