Allele Registry

Canonical Allele Identifier: PA284990

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059430

RCV001339387

RCV001781396

ClinVar Variation:

68556

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Val1619Met	CA284988 NM_006920.6:c.4855G>A