Canonical Allele Identifier: PA2827770652
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68609
ClinVar RCV Id: RCV000059486 RCV000519810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Gly968Arg
CA285111
NM_001353951.2:c.2902G>A
CA349060767
NM_001353951.2:c.2902G>C