Allele Registry

Canonical Allele Identifier: PA2827772071

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636288

ClinVar Variation:

530427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Asp1855Gly	CA16602232 NM_001353951.2:c.5564A>G