Allele Registry

Canonical Allele Identifier: PA107637

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059423

RCV003588568

ClinVar Variation:

68549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly1480Val	CA145243 NM_001165963.4:c.4439G>T