Allele Registry

Canonical Allele Identifier: PA2829676451

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002043796

ClinVar Variation:

1519829

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Asn1736Lys	CA349068416 NM_006920.6:c.5208C>A CA349068418 NM_006920.6:c.5208C>G