Canonical Allele Identifier: PA891861685
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 570034
ClinVar RCV Id: RCV000690797 RCV001771949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Ala339Thr
CA5252899
NM_001114753.3:c.1015G>A