Allele Registry

Canonical Allele Identifier: PA645405336

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414318

ClinVar Variation:

372740

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Pro1855Leu	CA16042429 NM_001165963.4:c.5564C>T