Canonical Allele Identifier: PA2827790794
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68573
ClinVar RCV Id: RCV000059449 RCV000189020 RCV002470754
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Ile1108Thr
CA285030
NM_001353961.2:c.3323T>C