Allele Registry

Canonical Allele Identifier: PA2827754763

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059441

ClinVar Variation:

68566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Thr1721Arg	CA285009 NM_001353948.2:c.5162C>G