Allele Registry

Canonical Allele Identifier: PA916036567

Gene: SCN1A HGNC NCBI

ClinVar Allele:

201418

ClinVar RCV:

RCV001200251

RCV001318625

ClinVar Variation:

206732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Ile1955Met	CA317108 NM_001353948.2:c.5865A>G