Canonical Allele Identifier: PA2827790296
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189882
ClinVar RCV Id: RCV000180835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg132Pro
CA303197
NM_001353961.2:c.395G>C