Allele Registry

Canonical Allele Identifier: PA2827756237

Gene: SCN1A HGNC NCBI

ClinVar Allele:

421314

ClinVar RCV:

RCV000494282

RCV000796912

ClinVar Variation:

430305

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Thr199Ile	CA349075265 NM_001353949.2:c.596C>T