Canonical Allele Identifier: PA2825158696
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195616
ClinVar RCV Id: RCV002628810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Pro169Leu
CA377030238
NM_000399.5:c.506C>T