Canonical Allele Identifier: PA2825821485
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246013
ClinVar RCV Id: RCV000236817 RCV000858272 RCV001094002 RCV002365227 RCV003955388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.Thr215Met
CA5517251
NM_001136177.1:c.644C>T