Canonical Allele Identifier: PA916036876
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg782Cys
CA145250
NM_001353961.2:c.2344C>T