Canonical Allele Identifier: PA2825821437
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2902563
ClinVar RCV Id: RCV003740819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.Gly179Arg
CA377030090
NM_001136177.1:c.535G>C
CA377030092
NM_001136177.1:c.535G>A