Canonical Allele Identifier: PA2826260839
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ile1961Thr
CA317678
NM_001202435.3:c.5882T>C