Allele Registry

Canonical Allele Identifier: PA317568

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188989

RCV003753105

ClinVar Variation:

206855

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Met1665Ile	CA317565 NM_001165963.4:c.4995G>A CA349069812 NM_001165963.4:c.4995G>T CA349069815 NM_001165963.4:c.4995G>C