Allele Registry

Canonical Allele Identifier: PA145238

Gene: SCN1A HGNC NCBI

ClinVar Allele:

79404

ClinVar RCV:

RCV000059384

RCV000180909

ClinVar Variation:

68512

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Ser626Gly	CA145235 NM_006920.6:c.1876A>G