Allele Registry

Canonical Allele Identifier: PA916036510

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414318

ClinVar Variation:

372740

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Pro1855Leu	CA16042429 NM_001353948.2:c.5564C>T