Canonical Allele Identifier: PA2827787688
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2032918
ClinVar RCV Id: RCV002881533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Cys351Gly
CA349071404
NM_001353960.2:c.1051T>G