Allele Registry

Canonical Allele Identifier: PA107870

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059502

RCV001385513

ClinVar Variation:

68624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Leu1287Pro	CA285150 NM_001165963.4:c.3860T>C