Allele Registry

Canonical Allele Identifier: PA2827760107

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059414

RCV001048734

ClinVar Variation:

68540

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Tyr1411Cys	CA284949 NM_001353949.2:c.4232A>G