Allele Registry

Canonical Allele Identifier: PA284879

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059381

ClinVar Variation:

68509

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Tyr413Asn	CA284877 NM_006920.6:c.1237T>A