Allele Registry

Canonical Allele Identifier: PA317492

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188960

RCV001999963

RCV003588594

ClinVar Variation:

206836

1452748

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly1515Arg	CA317489 NM_001165963.4:c.4543G>A CA349048633 NM_001165963.4:c.4543G>C