Allele Registry

Canonical Allele Identifier: PA645402643

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000498818

RCV001857000

ClinVar Variation:

431844

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Asn211Ser	CA349074293 NM_006920.6:c.632A>G