Canonical Allele Identifier: PA2825821662
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 651155
ClinVar RCV Id: RCV000806454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.Pro316Leu
CA377028313
NM_001136177.1:c.947C>T