Allele Registry

Canonical Allele Identifier: PA108654

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059392

RCV000255485

RCV000695650

RCV000763463

ClinVar Variation:

68520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Tyr84Cys	CA284901 NM_001165963.4:c.251A>G