Allele Registry

Canonical Allele Identifier: PA108023

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059444

RCV001854242

ClinVar Variation:

68569

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Met1780Thr	CA285018 NM_001165963.4:c.5339T>C