Allele Registry

Canonical Allele Identifier: PA317770

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189076

RCV001060675

ClinVar Variation:

206932

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.His324Arg	CA317767 NM_006920.6:c.971A>G