Allele Registry

Canonical Allele Identifier: PA2827780879

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000471658

ClinVar Variation:

408934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Ser1761Tyr	CA16610233 NM_001353955.2:c.5282C>A