Canonical Allele Identifier: PA209997
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206978
ClinVar RCV Id: RCV000189127 RCV000417104 RCV000195526 RCV002433854
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ser987Ile
CA209995
NM_021007.3:c.2960G>T