Allele Registry

Canonical Allele Identifier: PA2826011635

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001195991

RCV002280166

ClinVar Variation:

930374

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Ile227Thr	CA349074069 NM_001165964.3:c.680T>C