Allele Registry

Canonical Allele Identifier: PA2826260775

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000466422

ClinVar Variation:

408935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ile1922Ser	CA16610266 NM_001202435.3:c.5765T>G