Canonical Allele Identifier: PA658659767
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 458346
ClinVar RCV Id: RCV000579346 RCV002231266 RCV003989113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Met1Arg