Canonical Allele Identifier: PA2826581550
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458332
ClinVar RCV Id: RCV000547986 RCV002367790
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Cys230Tyr
CA374978391
NM_001278138.2:c.689G>A