Allele Registry

Canonical Allele Identifier: PA303597

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180984

ClinVar Variation:

190028

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Tyr1274Ser	CA303594 NM_001165963.4:c.3821A>C