Canonical Allele Identifier: PA2827769967
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1311030
ClinVar RCV Id: RCV001758539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ala442Gly
CA349070502
NM_001353951.2:c.1325C>G