Canonical Allele Identifier: PA891861681
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 583280
ClinVar RCV Id: RCV002233723 RCV002493252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Met269Val
CA374983063
NM_001114753.3:c.805A>G