Canonical Allele Identifier: PA915978014
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 569402
ClinVar RCV Id: RCV000690020
ClinVar Variation Id: 952193
ClinVar RCV Id: RCV001224254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Cys400Ser
CA377027376
NM_001136178.1:c.1199G>C
CA377027380
NM_001136178.1:c.1198T>A