Canonical Allele Identifier: PA2825822008
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 195071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Pro148Ser
CA241342
NM_001136178.1:c.442C>T