Canonical Allele Identifier: PA2827765773
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1490559
ClinVar RCV Id: RCV002001790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Val1158Gly
CA349056679
NM_001353950.2:c.3473T>G