Allele Registry

Canonical Allele Identifier: PA107416

Gene: SCN1A HGNC NCBI

ClinVar Allele:

79430

ClinVar RCV:

RCV000059412

RCV002513780

ClinVar Variation:

68538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Cys1396Gly	CA284943 NM_001165963.4:c.4186T>G