Allele Registry

Canonical Allele Identifier: PA916036928

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188989

RCV003753105

ClinVar Variation:

206855

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met851Ile	CA317565 NM_001353961.2:c.2553G>A CA349069812 NM_001353961.2:c.2553G>T CA349069815 NM_001353961.2:c.2553G>C