Allele Registry

Canonical Allele Identifier: PA284996

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059435

ClinVar Variation:

68560

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Thr1647Arg	CA284994 NM_006920.6:c.4940C>G