Allele Registry

Canonical Allele Identifier: PA256604

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000013751

RCV000059501

RCV002513023

ClinVar Variation:

12891

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Lys1259Thr	CA256602 NM_006920.6:c.3776A>C