Canonical Allele Identifier: PA2827776896
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68617
ClinVar RCV Id: RCV000059494
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Thr1198Lys
CA285129
NM_001353954.2:c.3593C>A