Canonical Allele Identifier: PA2827778599
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408928
ClinVar RCV Id: RCV000476602
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ile252Thr
CA16610165
NM_001353955.2:c.755T>C