Canonical Allele Identifier: PA2825822541
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 195071
ClinVar RCV Id: RCV000175594 RCV000797593 RCV002326956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129651.1:p.Pro98Ser
CA241342
NM_001136179.1:c.292C>T