Canonical Allele Identifier: PA645496244
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 300278
ClinVar RCV Id: RCV000268961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Leu181Phe
CA10635583
NM_000399.5:c.541C>T