Canonical Allele Identifier: PA891861708
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 582079
ClinVar RCV Id: RCV000706057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ser576Gly
CA374973482
NM_001114753.3:c.1726A>G