Allele Registry

Canonical Allele Identifier: PA916036945

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187721

ClinVar RCV:

RCV000180982

ClinVar Variation:

190026

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Gly874Val	CA303590 NM_001353961.2:c.2621G>T