Allele Registry

Canonical Allele Identifier: PA658659154

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530855

ClinVar Variation:

461256

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Leu890Pro	CA349061630 NM_001165963.4:c.2669T>C