Allele Registry

Canonical Allele Identifier: PA2829676307

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001971003

ClinVar Variation:

1474062

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Thr1647Ser	CA349069931 NM_006920.6:c.4939A>T