Canonical Allele Identifier: PA2826259286
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_001189364.1:p.Gly979Arg
CA285111
NM_001202435.3:c.2935G>A
CA349060767
NM_001202435.3:c.2935G>C