Allele Registry

Canonical Allele Identifier: PA2827788359

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530855

ClinVar Variation:

461256

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Leu861Pro	CA349061630 NM_001353960.2:c.2582T>C