Canonical Allele Identifier: PA658659870
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458329
ClinVar RCV Id: RCV002231257
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Arg406His
CA5252844
NM_001114753.3:c.1217G>A