Allele Registry

Canonical Allele Identifier: PA108602

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059530

RCV000465483

RCV000501085

ClinVar Variation:

68650

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Tyr1694Cys	CA285210 NM_001165963.4:c.5081A>G