Canonical Allele Identifier: PA2825044986
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 582079
ClinVar RCV Id: RCV000706057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Ser576Gly
CA374973482
NM_000118.3:c.1726A>G