Allele Registry

Canonical Allele Identifier: PA2827789032

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Cys1325Ser	CA16603838 NM_001353960.2:c.3974G>C CA349050657 NM_001353960.2:c.3973T>A