Canonical Allele Identifier: PA1139675618
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 982483
ClinVar RCV Id: RCV001262076 RCV001880033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Leu299Arg
CA374982466
NM_001114753.3:c.896T>G