Canonical Allele Identifier: PA2825158930
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2852587
ClinVar RCV Id: RCV003742205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Thr393Ser
CA377027423
NM_000399.5:c.1178C>G
CA377027424
NM_000399.5:c.1177A>T