Canonical Allele Identifier: PA916036828
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gln675Lys
CA256608
NM_001353961.2:c.2023C>A