Allele Registry

Canonical Allele Identifier: PA645405459

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000466422

ClinVar Variation:

408935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ile1922Ser	CA16610266 NM_001165963.4:c.5765T>G