Canonical Allele Identifier: PA101230
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 937612
ClinVar RCV Id: RCV001206664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Met269Arg
CA374983056
NM_001114753.3:c.806T>G