Allele Registry

Canonical Allele Identifier: PA317188

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188856

RCV000677680

RCV000986909

ClinVar Variation:

206755

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Gly329Val	CA317185 NM_006920.6:c.986G>T