Canonical Allele Identifier: PA645496240
Gene: EGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430425
ClinVar RCV Id: RCV000493614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000390.2:p.Pro103Leu
CA377031547
NM_000399.5:c.308C>T