Allele Registry

Canonical Allele Identifier: PA2826259636

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187764

ClinVar RCV:

RCV000180832

ClinVar Variation:

189879

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ala1255Pro	CA303188 NM_001202435.3:c.3763G>C