Allele Registry

Canonical Allele Identifier: PA2826258926

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187813

ClinVar RCV:

RCV000180853

ClinVar Variation:

189901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Trp754Leu	CA303254 NM_001202435.3:c.2261G>T