Canonical Allele Identifier: PA658803098
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 528083
ClinVar RCV Id: RCV000633165 RCV001165467 RCV002292573 RCV002413813
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Glu284Lys
CA5252951
NM_001114753.3:c.850G>A