Canonical Allele Identifier: PA2827790888
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 331880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Glu1184Gln
CA10611199
NM_001353961.2:c.3550G>C