Canonical Allele Identifier: PA916009921
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 213200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Gly9Asp
CA325327
NM_001278138.2:c.26G>A