Allele Registry

Canonical Allele Identifier: PA2827778122

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000466422

ClinVar Variation:

408935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340883.1:p.Ile1910Ser	CA16610266 NM_001353954.2:c.5729T>G