Allele Registry

Canonical Allele Identifier: PA317491

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188960

RCV001999963

RCV003588594

ClinVar Variation:

206836

1452748

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Gly1504Arg	CA317489 NM_006920.6:c.4510G>A CA349048633 NM_006920.6:c.4510G>C