Allele Registry

Canonical Allele Identifier: PA2827771805

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000079588

RCV001823112

ClinVar Variation:

93656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Met1703Thr	CA266846 NM_001353951.2:c.5108T>C