Allele Registry

Canonical Allele Identifier: PA2826258297

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180977

ClinVar Variation:

190021

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Lys276Gln	CA303576 NM_001202435.3:c.826A>C