Allele Registry

Canonical Allele Identifier: PA303465

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187742

ClinVar RCV:

RCV000180931

RCV002516539

ClinVar Variation:

189976

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ser1471Phe	CA303462 NM_001165963.4:c.4412C>T