Allele Registry

Canonical Allele Identifier: PA2829675861

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000474675

ClinVar Variation:

408922

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Cys1343Phe	CA16610188 NM_006920.6:c.4028G>T