Allele Registry

Canonical Allele Identifier: PA2827766980

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000986878

ClinVar Variation:

202173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Ile1471Leu	CA275462 NM_001353950.2:c.4411A>C