Allele Registry

Canonical Allele Identifier: PA2827786723

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530416

ClinVar Variation:

461280

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Gly1697Asp	CA349068786 NM_001353958.2:c.5090G>A