Canonical Allele Identifier: PA107458
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68607
ClinVar RCV Id: RCV000059484 RCV001387943
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Cys959Arg
CA285105
NM_001165963.4:c.2875T>C