Canonical Allele Identifier: PA2825821733
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685761
ClinVar RCV Id: RCV002249928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.His384Gln
CA377027480
NM_001136177.1:c.1152C>A
CA377027482
NM_001136177.1:c.1152C>G