Allele Registry

Canonical Allele Identifier: PA916036840

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188960

RCV001999963

RCV003588594

ClinVar Variation:

206836

1452748

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Gly701Arg	CA317489 NM_001353961.2:c.2101G>A CA349048633 NM_001353961.2:c.2101G>C