Canonical Allele Identifier: PA101220
Gene: ENG HGNC NCBI

Linked Data

ClinVar Variation Id: 565357
ClinVar RCV Id: RCV002232818 RCV002442411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108225.1:p.Leu8Pro
CA374989640
NM_001114753.3:c.23T>C