Allele Registry

Canonical Allele Identifier: PA2826259129

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530855

ClinVar Variation:

461256

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Leu890Pro	CA349061630 NM_001202435.3:c.2669T>C