Canonical Allele Identifier: PA2826581704
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 407135
ClinVar RCV Id: RCV000458266 RCV003151063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Cys367Tyr
CA500023
NM_001278138.2:c.1100G>A