Canonical Allele Identifier: PA2827756334
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 265297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Leu221Val
CA10588324
NM_001353949.2:c.661C>G