Canonical Allele Identifier: PA2825044692
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1000011
ClinVar RCV Id: RCV001296084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Arg399Gly
CA374978558
NM_000118.3:c.1195A>G