Canonical Allele Identifier: PA2828470417
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1693057
ClinVar RCV Id: RCV002259484
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Tyr110His
CA349011583
NM_001371246.1:c.328T>C