Canonical Allele Identifier: PA2826581569
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 652180
ClinVar RCV Id: RCV000807687 RCV003279087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265067.1:p.Ala243Glu
CA374978152
NM_001278138.2:c.728C>A