Canonical Allele Identifier: PA1139689176
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 958313
ClinVar RCV Id: RCV001231456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ala201Ser
CA377029759
NM_001136178.1:c.601G>T