Canonical Allele Identifier: PA2826581745
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_001265067.1:p.Ser394Gly
CA374973482
NM_001278138.2:c.1180A>G