Canonical Allele Identifier: PA2827067674
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2827590
ClinVar RCV Id: RCV003741912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307966.1:p.Pro319Arg
CA377027707
NM_001321037.2:c.956C>G