Canonical Allele Identifier: PA645400307
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 419983
ClinVar RCV Id: RCV000478361 RCV003593964
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Val236del
CA16618751
NM_001114753.3:c.706_708del