Allele Registry

Canonical Allele Identifier: PA2826013197

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Cys1326Ser	CA16603838 NM_001165964.3:c.3977G>C CA349050657 NM_001165964.3:c.3976T>A