Allele Registry

Canonical Allele Identifier: PA2827786812

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000471658

ClinVar Variation:

408934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Ser1745Tyr	CA16610233 NM_001353958.2:c.5234C>A