Allele Registry

Canonical Allele Identifier: PA2827790702

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189008

RCV001067049

ClinVar Variation:

206870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met1042Thr	CA317625 NM_001353961.2:c.3125T>C