Allele Registry

Canonical Allele Identifier: PA2827789274

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000986878

ClinVar Variation:

202173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Ile1453Leu	CA275462 NM_001353960.2:c.4357A>C