Allele Registry

Canonical Allele Identifier: PA281750

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000022764

RCV001379443

ClinVar Variation:

29883

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Ala1658Glu	CA281748 NM_006920.6:c.4973C>A