Canonical Allele Identifier: PA915977874
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373129
ClinVar RCV Id: RCV000413410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Ser155Phe
CA16042727
NM_001136178.1:c.464C>T