Canonical Allele Identifier: PA2499238135
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1000011
ClinVar RCV Id: RCV001296084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg399Gly
CA374978558
NM_001114753.3:c.1195A>G