Canonical Allele Identifier: PA645400386
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407125
ClinVar RCV Id: RCV002261089 RCV003153610
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Val568Ile
CA5252675
NM_001114753.3:c.1702G>A