Canonical Allele Identifier: PA2825821998
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1346724
ClinVar RCV Id: RCV002030160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ala139Ser
CA377030723
NM_001136178.1:c.415G>T