Allele Registry

Canonical Allele Identifier: PA2827761996

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000466422

ClinVar Variation:

408935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Ile1911Ser	CA16610266 NM_001353949.2:c.5732T>G