Allele Registry

Canonical Allele Identifier: PA317755

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189072

RCV000636394

RCV001252613

ClinVar Variation:

206928

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Glu158Gln	CA317752 NM_006920.6:c.472G>C