Canonical Allele Identifier: PA645496197
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246186
ClinVar RCV Id: RCV000235956 RCV000527649 RCV001094067 RCV001658082 RCV002225532 RCV002411070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Met64Ile
CA5517310
NM_000399.5:c.192G>C
CA377032540
NM_000399.5:c.192G>T
CA377032547
NM_000399.5:c.192G>A