Canonical Allele Identifier: PA356429
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219844
ClinVar RCV Id: RCV000206846 RCV000431412 RCV000999872
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Amino-acid Alleles

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