Allele Registry

Canonical Allele Identifier: PA2827777068

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000483132

ClinVar Variation:

421599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340883.1:p.Lys1301Thr	CA16617296 NM_001353954.2:c.3902A>C