Canonical Allele Identifier: PA2825822017
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141192
ClinVar RCV Id: RCV003056833 RCV003482437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Thr157Ser
CA5517271
NM_001136178.1:c.469A>T
CA377030428
NM_001136178.1:c.470C>G