Canonical Allele Identifier: PA2827778188
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ile1949Thr
CA317678
NM_001353954.2:c.5846T>C