Canonical Allele Identifier: PA2825158861
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 651155
ClinVar RCV Id: RCV000806454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Pro316Leu
CA377028313
NM_000399.5:c.947C>T