Canonical Allele Identifier: PA2826581532
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1000011
ClinVar RCV Id: RCV001296084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Arg217Gly
CA374978558
NM_001278138.2:c.649A>G