Allele Registry

Canonical Allele Identifier: PA356429

Gene: EGR2 HGNC NCBI

ClinVar RCV:

RCV000206846

RCV000431412

RCV000999872

ClinVar Variation:

219844

HGVS (amino-acid)	Matching Registered Transcripts
NP_000390.2:p.Arg409Gln	CA350841 NM_000399.5:c.1226G>A