Allele Registry

Canonical Allele Identifier: PA108716

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000013756

RCV000013757

ClinVar Variation:

12895

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Val1611Phe	CA256614 NM_001165963.4:c.4831G>T