Canonical Allele Identifier: PA2827771495
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 853086
ClinVar RCV Id: RCV001057828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Met1522Lys
CA349072346
NM_001353951.2:c.4565T>A