Canonical Allele Identifier: PA104278
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16750
ClinVar RCV Id: RCV001049422 RCV003482227 RCV000018234
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Arg409Trp
CA341431
NM_000399.5:c.1225C>T