Canonical Allele Identifier: PA2826014173
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ile1894Thr
CA285030
NM_001165964.3:c.5681T>C