Canonical Allele Identifier: PA2825821356
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430425
ClinVar RCV Id: RCV000493614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.Pro103Leu
CA377031547
NM_001136177.1:c.308C>T