Allele Registry

Canonical Allele Identifier: PA108579

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059414

RCV001048734

ClinVar Variation:

68540

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Tyr1422Cys	CA284949 NM_001165963.4:c.4265A>G