Allele Registry

Canonical Allele Identifier: PA2827788267

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180925

ClinVar Variation:

189971

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Tyr798Asp	CA303448 NM_001353960.2:c.2392T>G