Canonical Allele Identifier: PA891848306
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 567919
ClinVar RCV Id: RCV000688129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg220Gly
CA349017486
NM_021007.3:c.658A>G