Allele Registry

Canonical Allele Identifier: PA2827783649

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000022764

RCV001379443

ClinVar Variation:

29883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Ala1641Glu	CA281748 NM_001353957.2:c.4922C>A