Canonical Allele Identifier: PA2826014258
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Arg1960Gln
CA1942622
NM_001165964.3:c.5879G>A