Allele Registry

Canonical Allele Identifier: PA303386

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180902

RCV001531324

ClinVar Variation:

189949

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ser872Tyr	CA303383 NM_001165963.4:c.2615C>A