Allele Registry

Canonical Allele Identifier: PA108398

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059441

ClinVar Variation:

68566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Thr1721Arg	CA285009 NM_001165963.4:c.5162C>G