Allele Registry

Canonical Allele Identifier: PA2826012634

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636437

RCV001384352

ClinVar Variation:

530535

1071810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Glu926Asp	CA349061108 NM_001165964.3:c.2778G>C CA349061111 NM_001165964.3:c.2778G>T