Canonical Allele Identifier: PA257571
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 16673
ClinVar RCV Id: RCV000018153 RCV002433460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Met1Thr