Allele Registry

Canonical Allele Identifier: PA2827789783

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000471658

ClinVar Variation:

408934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Ser1744Tyr	CA16610233 NM_001353960.2:c.5231C>A