Allele Registry

Canonical Allele Identifier: PA2827779121

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000417000

ClinVar Variation:

375511

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Glu615Asp	CA16044314 NM_001353955.2:c.1845G>C CA349067460 NM_001353955.2:c.1845G>T