Allele Registry

Canonical Allele Identifier: PA242666

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000176636

RCV001852177

ClinVar Variation:

195946

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Asn1768Asp	CA242664 NM_006920.6:c.5302A>G