Allele Registry

Canonical Allele Identifier: PA2826260546

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000471658

ClinVar Variation:

408934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ser1773Tyr	CA16610233 NM_001202435.3:c.5318C>A