Canonical Allele Identifier: PA2825356799
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 894363
ClinVar RCV Id: RCV001134807 RCV001531928 RCV002558290
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ile1592Thr
CA1940318
NM_001040142.2:c.4775T>C