Canonical Allele Identifier: PA1139689170
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 863169
ClinVar RCV Id: RCV001070072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Pro167Leu
CA377030268
NM_001136178.1:c.500C>T