Allele Registry

Canonical Allele Identifier: PA2827771170

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Cys1343Ser	CA16603838 NM_001353951.2:c.4028G>C CA349050657 NM_001353951.2:c.4027T>A