Allele Registry

Canonical Allele Identifier: PA303266

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180856

ClinVar Variation:

189904

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Gly177Val	CA303263 NM_006920.6:c.530G>T