Canonical Allele Identifier: PA317680
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ile1950Thr
CA317678
NM_006920.6:c.5849T>C