Canonical Allele Identifier: PA2825158692
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 863169
ClinVar RCV Id: RCV001070072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Pro167Leu
CA377030268
NM_000399.5:c.500C>T