Canonical Allele Identifier: PA101561
Gene: ENO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001967.3:p.Gly156Asp
CA126730
NM_001976.5:c.467G>A