Canonical Allele Identifier: PA2826260392
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68649
ClinVar RCV Id: RCV000059529 RCV002514308
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Phe1692Ser
CA285207
NM_001202435.3:c.5075T>C