Canonical Allele Identifier: PA2827771705
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68645
ClinVar RCV Id: RCV000059525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Met1653Lys
CA285198
NM_001353951.2:c.4958T>A