Allele Registry

Canonical Allele Identifier: PA2826259801

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Cys1354Ser	CA16603838 NM_001202435.3:c.4061G>C CA349050657 NM_001202435.3:c.4060T>A