Canonical Allele Identifier: PA2573161523
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 1477415
ClinVar RCV Id: RCV002018733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000109.1:p.Arg618Pro
CA374971499
NM_000118.3:c.1853G>C