Canonical Allele Identifier: PA2825822326
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1807345
ClinVar RCV Id: RCV002475302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129650.1:p.Phe398Leu
CA377027386
NM_001136178.1:c.1194C>G
CA377027387
NM_001136178.1:c.1194C>A
CA377027392
NM_001136178.1:c.1192T>C