Canonical Allele Identifier: PA645400354
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407115
ClinVar RCV Id: RCV000462769 RCV000791420 RCV001531114 RCV002379438
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Gly331Ser
CA16612528
NM_001114753.3:c.991G>A