Canonical Allele Identifier: PA2828476478
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2575847
ClinVar RCV Id: RCV003321413
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Gly1642Ala
CA349037801
NM_001371247.1:c.4925G>C