Allele Registry

Canonical Allele Identifier: PA2827785179

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180852

ClinVar Variation:

189900

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Trp710Leu	CA303250 NM_001353958.2:c.2129G>T