Allele Registry

Canonical Allele Identifier: PA645404198

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Cys1354Ser	CA16603838 NM_001165963.4:c.4061G>C CA349050657 NM_001165963.4:c.4060T>A