Allele Registry

Canonical Allele Identifier: PA104268

Gene: EGR2 HGNC NCBI

ClinVar Allele:

49430

ClinVar RCV:

RCV000033901

RCV000701335

RCV000789745

RCV002472942

ClinVar Variation:

41008

HGVS (amino-acid)	Matching Registered Transcripts
NP_000390.2:p.Arg381His	CA343874 NM_000399.5:c.1142G>A