Allele Registry

Canonical Allele Identifier: PA2826014175

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000466422

ClinVar Variation:

408935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Ile1894Ser	CA16610266 NM_001165964.3:c.5681T>G