Canonical Allele Identifier: PA915976850
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 810423
ClinVar RCV Id: RCV000999220 RCV001069948 RCV002481795
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Thr617Met
CA5252620
NM_001114753.3:c.1850C>T