Allele Registry

Canonical Allele Identifier: PA2827761519

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000471658

ClinVar Variation:

408934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Ser1762Tyr	CA16610233 NM_001353949.2:c.5285C>A