Allele Registry

Canonical Allele Identifier: PA645402639

Gene: SCN1A HGNC NCBI

ClinVar Allele:

421314

ClinVar RCV:

RCV000494282

RCV000796912

ClinVar Variation:

430305

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Thr199Ile	CA349075265 NM_006920.6:c.596C>T