Canonical Allele Identifier: PA915977952
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 651155
ClinVar RCV Id: RCV000806454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Pro316Leu
CA377028313
NM_001136178.1:c.947C>T