Allele Registry

Canonical Allele Identifier: PA2827776179

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180966

ClinVar Variation:

190010

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340883.1:p.Pro656Leu	CA303541 NM_001353954.2:c.1967C>T