Canonical Allele Identifier: PA2825822340
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1748571
ClinVar RCV Id: RCV002344900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Tyr402Cys
CA377027361
NM_001136178.1:c.1205A>G