Canonical Allele Identifier: PA2825579043
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 2848235
ClinVar RCV Id: RCV003758553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ala111Thr
CA5253159
NM_001114753.3:c.331G>A