Canonical Allele Identifier: PA317931
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206988
ClinVar RCV Id: RCV000189137 RCV000795173 RCV002288794
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Glu1162Val
CA317930
NM_001040142.2:c.3485A>T