Canonical Allele Identifier: PA2827779292
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1701394
ClinVar RCV Id: RCV002276082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Thr770Ile
CA349064114
NM_001353955.2:c.2309C>T