Allele Registry

Canonical Allele Identifier: PA916036516

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636288

ClinVar Variation:

530427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Asp1866Gly	CA16602232 NM_001353948.2:c.5597A>G