Allele Registry

Canonical Allele Identifier: PA284930

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059404

RCV001344646

ClinVar Variation:

68531

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Gly1222Arg	CA284928 NM_006920.6:c.3664G>C