Canonical Allele Identifier: PA2825158907
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2827590
ClinVar RCV Id: RCV003741912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Pro369Arg
CA377027707
NM_000399.5:c.1106C>G