Canonical Allele Identifier: PA2825821771
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011752
ClinVar RCV Id: RCV001309600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129649.1:p.Ala408Ser
CA377027319
NM_001136177.1:c.1222G>T