Allele Registry

Canonical Allele Identifier: PA916036934

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000022764

RCV001379443

ClinVar Variation:

29883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ala855Glu	CA281748 NM_001353961.2:c.2564C>A