Allele Registry

Canonical Allele Identifier: PA2827766281

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000483132

ClinVar Variation:

421599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Lys1302Thr	CA16617296 NM_001353950.2:c.3905A>C