Canonical Allele Identifier: PA916036810
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68545
ClinVar RCV Id: RCV000059419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Tyr648Cys
CA284964
NM_001353961.2:c.1943A>G