Canonical Allele Identifier: PA2826581549
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1040195
ClinVar RCV Id: RCV001343795
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Cys230Gly
CA374978392
NM_001278138.2:c.688T>G