Canonical Allele Identifier: PA2827783866
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68659
ClinVar RCV Id: RCV000059539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ile1754Met
CA285234
NM_001353957.2:c.5262C>G