Canonical Allele Identifier: PA2825822609
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 300278
ClinVar RCV Id: RCV000268961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129651.1:p.Leu131Phe
CA10635583
NM_001136179.1:c.391C>T