Allele Registry

Canonical Allele Identifier: PA145234

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059382

ClinVar Variation:

68510

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Val422Glu	CA145232 NM_006920.6:c.1265T>A