Canonical Allele Identifier: PA2827067629
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 651155
ClinVar RCV Id: RCV000806454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Pro266Leu
CA377028313
NM_001321037.2:c.797C>T