Canonical Allele Identifier: PA2573179527
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1468735
ClinVar RCV Id: RCV001969143
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Thr369Ile
CA5252878
NM_001114753.3:c.1106C>T