Canonical Allele Identifier: PA325329
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 213200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Gly191Asp
CA325327
NM_001114753.3:c.572G>A