Allele Registry

Canonical Allele Identifier: PA2826257915

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180979

ClinVar Variation:

190023

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ala24Thr	CA303581 NM_001202435.3:c.70G>A